History
# Registration date Revision Id
3 2021-02-16, 1399/11/28 174724
2 2021-01-09, 1399/10/20 166686
1 2020-06-10, 1399/03/21 138285
Changes made to previous revision
  • Help:

    Red color represents old content. It may be empty showing addition in the new version.
    Green color represents new content. It may be empty showing deletion in the new version.

    Inline Side by side
    Added new contents, deleted old contents, contents that are not changed.
    New table contents New table contents
    Old table contents Old table contents
    Unchanged contents Unchanged contents
    Added new contents, contents that are not changed.
    Deleted old contents, contents that are not changed.
    Old table contents Old table contents
    Unchanged contents Unchanged contents
    New table contents New table contents
    Unchanged contents Unchanged contents
  • Protocol summary

    In this intervention study, 60 children with asthma who have the criteria to enter the study, are divided into two groups of 30 patients by block randomization method. Individuals' parents are explained about treatment methods and their benefits and complications, and informed consent is obtained
    In this double-blind clinical trial, phase 2, 60 children with asthma who have the inclusion criteria are placed in 2 parallel groups of 30 patients using a table of random numbers
    در اين مطالعه مداخله ای 60 کودک مبتلا به آسم که دارای معیارهای ورود به مطالعه هستند، از روش تصادفی سازی بلوکی در دو گروه 30 نفری قرار می گیرند. به والدین افراد درمورد روشهای درمان و مزايا و عوارض آنها توضیح داده شده و رضايت آگاهانه اخذ میشود. .
    در اين کارآزمایی بالینی دو سو کور، فاز 2، 60 کودک مبتلا به آسم که دارای معیارهای ورود به مطالعه هستند، با روش تصـادفي سـازي ساده با استفاده از جدول اعداد تصادفي در دو گروه 30 نفری در گروه های موازی شرکت خواهند نمود.
    In this study, 60 children with asthma aged 5 to 12 years who referred to the allergy clinic of Ardabil University of Medical Sciences were randomly divided into two groups (30 patients in each group). After obtaining written consent from the parents, general information and cough and fever, wheezing and other symptoms of respiratory infection will be collected. For one week, the dried thyme extract test group will be given a dose of 1 to 4 grams per kilogram per day in 3 divided doses along with routine medical treatment, and the control group will receive only routine medical treatment.
    In this study, 60 children with asthma aged 5 to 12 years who referred to the allergy clinic of Ardabil University of Medical Sciences were randomly divided into two groups (30 patients in each group). After obtaining written consent from the parents, general information and cough and fever, wheezing and other symptoms of respiratory infection will be collected. Patients in the intervention group will be given 1 to 4 grams of dried thyme leaf powder prepared as a syrup for a week, at a dose of 20 mg / kg every 8 hours along with routine medical treatment, and the control group will receive routine medical treatment and 2 cc placebo syrup .
    در این مطالعه 60 نفر از کودکان مبتلا به آسم 5 تا 12 سال مراجعه کننده به کلینیک آلرژی دانشگاه علوم پزشکی اردبیل بطور تصادفی در دو گروه قرار می گیرند ( 30 بیمار در هر گروه) . پس از اخذ رضایت نامه كتبي از والدین، اطلاعات عمومی و سرفه و تب،خس خس سینه و سایر علائم عفونت تنفسی جمع آوری خواهد شد. به مدت یک هفته به گروه آزمایش عصاره خشک آویشن با دوز 1 تا 4 گرم بر کیلو گرم در روز در 3 دوز منقسم در کنار درمان طبی روتین بیماری داده خواهد شد و گروه شاهد فقط درمان طبی روتین را دریافت خواهد کرد.
    در این مطالعه 60 نفر از کودکان مبتلا به آسم 5 تا 12 سال مراجعه کننده به کلینیک آلرژی دانشگاه علوم پزشکی اردبیل بطور تصادفی در دو گروه قرار می گیرند ( 30 بیمار در هر گروه) . پس از اخذ رضایت نامه كتبي از والدین، اطلاعات عمومی و سرفه و تب،خس خس سینه و سایر علائم عفونت تنفسی جمع آوری خواهد شد. به مدت یک هفته به گروه آزمایش ۱ تا ۴ گرم پودر برگه خشک شده آویشن آماده شده بصورت شربت، با دوز 20 میلی گرم بر کیلو گرم هر 8 ساعت در کنار درمان طبی روتین بیماری داده خواهد شد و گروه شاهد درمان طبی روتین و 2 سی سی پلاسبو را دریافت خواهد کرد.
    Intervention group: Patients in the intervention group will be given dried thyme extract for 1 week at a dose of 1 to 4 grams per kilogram per day in 3 divided doses along with routine medical treatment. Control group: The control group will only receive routine medical treatment
    Intervention group: Patients in the intervention group will be given 1 to 4 grams of dried thyme leaf powder prepared as a syrup for a week, at a dose of 20 mg / kg every 8 hours, along prednisolone tablets (1 mg / kg, daily, Abureyhan Co.), salbutamol spray (2 puffs every 3 hours by Caspian Tamin Co), theophylline syrup (4 cc every 6 hours by Elixir Co) with routine medical treatment.. Control group: The control group will receive 2 cc placebo syrup and prednisolone tablets (1 mg / kg, daily, Abureyhan Co.), salbutamol spray (2 puffs every 3 hours by Caspian Tamin Co), theophylline syrup (4 cc every 6 hours by Elixir Co).
    گروه مداخله: به بیماران گروه مداخله به مدت یک هفته عصاره خشک آویشن با دوز 1 تا 4 گرم بر کیلو گرم در روز در 3 دوز منقسم در کنار درمان طبی روتین بیماری داده خواهد شد. گروه کنترل: گروه کنترل فقط درمان طبی روتین را دریافت خواهد کرد.
    گروه مداخله: به بیماران گروه مداخله به مدت یک هفته ۱ تا ۴ گرم پودر برگه خشک شده آویشن آماده شده بصورت شربت، با دوز 20 میلی گرم بر کیلو گرم هر 8 ساعت در کنار قرص پردنیزولون (یک میلی گرم بر کیلوگرم، روزانه، محصول شرکت ابوریحان)، اسپری سالبوتامول ( 2 پاف هر 3 ساعت محصول شرکت کاسپین تامین)، شربت تئوفیلین ( 4 سی سی هر 6 ساعت محصول شرکت اکسیر) بیماری داده خواهد شد. گروه کنترل: گروه کنترل 2 سی سی شربت پلاسبو و قرص پردنیزولون (یک میلی گرم بر کیلوگرم، روزانه، محصول شرکت ابوریحان)، اسپری سالبوتامول ( 2 پاف هر 3 ساعت محصول شرکت کاسپین تامین)، شربت تئوفیلین ( 4 سی سی هر 6 ساعت محصول شرکت اکسیر) را دریافت خواهند کرد.
  • General information

    1
    1
    1-2
    2
    2021-02-20, 1399/12/02
    2021-06-22, 1400/04/01
    Patients will be randomly assigned to one of two identified groups through blockade.
    Randomization method is a simple randomizing using a table of random numbers, a set of numbers which is completely generated randomly without any specific pattern or order in a table form. Table numbers are read from the left, in a way that even numbers are assigned to intervention A and odd numbers to intervention B. In this way, the researcher touches one of the numbers and moves to the right, then records the numbers and assigns them to different groups. Next, considering the volume of the research sample, aluminum wrapper envelopes are prepared (in order not to clarify the content of the envelopes), each of the random sequences is recorded on a card and placed inside an envelope. To maintain a random sequence, envelopes are numbered in the same way. Finally, the flap of the envelopes are sealed and respectively placed inside a box. To reveal the participants' assigned group, at the beginning of the registration based on the order of eligible participants entry to study, one of the envelopes is opened.
    بیماران بصورت تخصیص تصادفی از طریق بلوک بندی در یکی از دو گروه مشخص شده قرار خواهد گرفت.
    روش تصادفی سازی، تصـادفي سـازي ساده با استفاده از جدول اعداد تصادفي، مجموعـه انبـوهي از اعداد است كه بدون الگو و يا نظم مشخصي و بـه صورت كاملاً تصادفي توليد شـده و بـه صـورت جدول در آمـده اسـت، خواهد بود. اعداد جدول از سمت چپ خوانده شده واعداد زوج براي مداخله A و اعداد فرد براي مداخلــه B در نظر گرفته می شود. به این صورت که محقق برروي يكي از اعداد دست ميگذارد و به سمت راست حركت كرده و اعداد را ثبت و به گروههاي مختلف تخصيص مـي دهـد. سپس به تعداد حجم نمونه پژوهش، پاكت نامه با لفـاف آلومينيومي (بـه منظـور عـدم وضـوح محتـواي پاكتها)، تهيه و هر يك از تـوالي هـاي تصـادفي ايجاد شده برروي يك كـارت ثبـت مـيشـود و كــارت هــا در داخــل پاكــتهــای نامــه بــه ترتيــب جاي گذاري مـي شـوند. بـه منظـور حفـظ تـوالي تصادفي نيز، بر روي سـطح خـارجي پاكـتهـا شماره گذاري به همان ترتيب انجام ميگيرد. در نهايت درب پاكتهای نامه چسبانده شـده و بـه ترتيب در داخل جعبه اي قرار ميگيرد. در زمان شروع ثبت نـام شـركت كننـدگان، براسـاس ترتيـب ورود شـركت كننـدگان واجـد شرايط به مطالعه، يكـي از پاكـتهـاي نامـه بـه ترتيـب بـاز شـده و گـروه تخصـيص يافتـه آن شركت كننده، آشكار ميگردد.
    Patients and outcome assessors are unaware of the type of intervention
    Due to the fact that placebo is used, patients and outcome assessors are unaware of the type of intervention.
    بیماران و ارزیابی کننده پیامد از نوع مداخله بی اطلاع می باشند.
    بیماران و ارزیابی کننده پیامد با توجه به اینکه از پلاسبو استفاده می گردد از نوع مداخله بی اطلاع می باشند.
  • Intervention groups

    #1
    Intervention group: For one week, the dried thyme extract will be given a dose of 1 to 4 grams per kilogram per day in 3 divided doses along with routine medical treatment.
    Intervention group: Patients in the intervention group will be given 1 to 4 grams of dried thyme leaf powder prepared as a syrup for a week, at a dose of 20 mg / kg every 8 hours, along prednisolone tablets (1 mg / kg, daily, Abureyhan Co.), salbutamol spray (2 puffs every 3 hours by Caspian Tamin Co), theophylline syrup (4 cc every 6 hours by Elixir Co) with routine medical treatment.
    گروه مداخله: به مدت یک هفته عصاره خشک آویشن با دوز 1 تا 4 گرم بر کیلو گرم در روز در 3 دوز منقسم در کنار درمان طبی روتین بیماری داده خواهد شد.
    گروه مداخله: به بیماران گروه مداخله به مدت یک هفته ۱ تا ۴ گرم پودر برگه خشک شده آویشن آماده شده بصورت شربت، با دوز 20 میلی گرم بر کیلو گرم هر 8 ساعت در کنار قرص پردنیزولون (یک میلی گرم بر کیلوگرم، روزانه، محصول شرکت ابوریحان)، اسپری سالبوتامول ( 2 پاف هر 3 ساعت محصول شرکت کاسپین تامین)، شربت تئوفیلین ( 4 سی سی هر 6 ساعت محصول شرکت اکسیر) بیماری داده خواهد شد.
    #2
    Control group: Control group will receive only routine medical treatment.
    Control group: Control group will receive 2 cc placebo syrup and prednisolone tablets (1 mg / kg, daily, Abureyhan Co.), salbutamol spray (2 puffs every 3 hours by Caspian Tamin Co), theophylline syrup (4 cc every 6 hours by Elixir Co) with routine medical treatment.
    گروه کنترل: فقط درمان طبی روتین را دریافت خواهد کرد. En .
    گروه کنترل: 2 سی سی پلاسبو و قرص پردنیزولون (یک میلی گرم بر کیلوگرم، روزانه، محصول شرکت ابوریحان)، اسپری سالبوتامول ( 2 پاف هر 3 ساعت محصول شرکت کاسپین تامین)، شربت تئوفیلین ( 4 سی سی هر 6 ساعت محصول شرکت اکسیر) بیماری داده خواهد شد.

Protocol summary

Study aim
Evaluation of the sedative effect of thyme in cough in children with asthma
Design
In this double-blind clinical trial, phase 2, 60 children with asthma who have the inclusion criteria are placed in 2 parallel groups of 30 patients using a table of random numbers
Settings and conduct
In this study, 60 children with asthma aged 5 to 12 years who referred to the allergy clinic of Ardabil University of Medical Sciences were randomly divided into two groups (30 patients in each group). After obtaining written consent from the parents, general information and cough and fever, wheezing and other symptoms of respiratory infection will be collected. Patients in the intervention group will be given 1 to 4 grams of dried thyme leaf powder prepared as a syrup for a week, at a dose of 20 mg / kg every 8 hours along with routine medical treatment, and the control group will receive routine medical treatment and 2 cc placebo syrup .
Participants/Inclusion and exclusion criteria
Having asthma, age between 5-12 years, Lack of chronic disability or illness. Exclusion criteria: Failure to complete the course of treatment
Intervention groups
Intervention group: Patients in the intervention group will be given 1 to 4 grams of dried thyme leaf powder prepared as a syrup for a week, at a dose of 20 mg / kg every 8 hours, along prednisolone tablets (1 mg / kg, daily, Abureyhan Co.), salbutamol spray (2 puffs every 3 hours by Caspian Tamin Co), theophylline syrup (4 cc every 6 hours by Elixir Co) with routine medical treatment.. Control group: The control group will receive 2 cc placebo syrup and prednisolone tablets (1 mg / kg, daily, Abureyhan Co.), salbutamol spray (2 puffs every 3 hours by Caspian Tamin Co), theophylline syrup (4 cc every 6 hours by Elixir Co).
Main outcome variables
cough

General information

Reason for update
Incomplete number of patients
Acronym
IRCT registration information
IRCT registration number: IRCT20200505047310N1
Registration date: 2020-06-10, 1399/03/21
Registration timing: prospective

Last update: 2021-03-11, 1399/12/21
Update count: 2
Registration date
2020-06-10, 1399/03/21
Registrant information
Name
Elnaz Eskandarpour
Name of organization / entity
Country
Iran (Islamic Republic of)
Phone
+98 45 3325 2251
Email address
e.eskandarpour@arums.ac.ir
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2020-08-22, 1399/06/01
Expected recruitment end date
2021-06-22, 1400/04/01
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
Evaluation of sedative effect of thyme on cough in children 5 to 12 years of age with asthma
Public title
Evaluation of the sedative effect of thyme in cough in children with asthma
Purpose
Treatment
Inclusion/Exclusion criteria
Inclusion criteria:
Having asthma age between 5-12 years Lack of chronic disability or illness
Exclusion criteria:
Failure to complete the course of treatment
Age
From 5 years old to 12 years old
Gender
Both
Phase
2
Groups that have been masked
  • Participant
  • Outcome assessor
Sample size
Target sample size: 60
Randomization (investigator's opinion)
Randomized
Randomization description
Randomization method is a simple randomizing using a table of random numbers, a set of numbers which is completely generated randomly without any specific pattern or order in a table form. Table numbers are read from the left, in a way that even numbers are assigned to intervention A and odd numbers to intervention B. In this way, the researcher touches one of the numbers and moves to the right, then records the numbers and assigns them to different groups. Next, considering the volume of the research sample, aluminum wrapper envelopes are prepared (in order not to clarify the content of the envelopes), each of the random sequences is recorded on a card and placed inside an envelope. To maintain a random sequence, envelopes are numbered in the same way. Finally, the flap of the envelopes are sealed and respectively placed inside a box. To reveal the participants' assigned group, at the beginning of the registration based on the order of eligible participants entry to study, one of the envelopes is opened.
Blinding (investigator's opinion)
Double blinded
Blinding description
Due to the fact that placebo is used, patients and outcome assessors are unaware of the type of intervention.
Placebo
Used
Assignment
Parallel
Other design features

Secondary Ids

empty

Ethics committees

1

Ethics committee
Name of ethics committee
Ethics committee of Ardabil University of Medical Sciences
Street address
Daneshghah Street
City
Ardabil
Province
Ardabil
Postal code
561577664
Approval date
2019-08-10, 1398/05/19
Ethics committee reference number
1398.242.IR.ARUMS.REC

Health conditions studied

1

Description of health condition studied
Asthma
ICD-10 code
J45
ICD-10 code description
Asthma

Primary outcomes

1

Description
cough
Timepoint
Before and after the intervention
Method of measurement
Medical examination

Secondary outcomes

1

Description
Fever
Timepoint
Before and after the intervention
Method of measurement
Thermometer

2

Description
wheezing
Timepoint
Before and after the intervention
Method of measurement
Medical Examination

Intervention groups

1

Description
Intervention group: Patients in the intervention group will be given 1 to 4 grams of dried thyme leaf powder prepared as a syrup for a week, at a dose of 20 mg / kg every 8 hours, along prednisolone tablets (1 mg / kg, daily, Abureyhan Co.), salbutamol spray (2 puffs every 3 hours by Caspian Tamin Co), theophylline syrup (4 cc every 6 hours by Elixir Co) with routine medical treatment.
Category
Treatment - Drugs

2

Description
Control group: Control group will receive 2 cc placebo syrup and prednisolone tablets (1 mg / kg, daily, Abureyhan Co.), salbutamol spray (2 puffs every 3 hours by Caspian Tamin Co), theophylline syrup (4 cc every 6 hours by Elixir Co) with routine medical treatment.
Category
Treatment - Drugs

Recruitment centers

1

Recruitment center
Name of recruitment center
Bu Ali Hospital
Full name of responsible person
Elnaz Eskandarpour
Street address
Moallem Street
City
Ardabil
Province
Ardabil
Postal code
۵۶۱۳۶۴۳۱۹۷
Phone
+98 45 3325 2251
Email
e.eskandarpour@arums.ac.ir

Sponsors / Funding sources

1

Sponsor
Name of organization / entity
Ardabil University of Medical Sciences
Full name of responsible person
Shahab Bohlooli
Street address
Daneshhah Street
City
Ardabil
Province
Ardabil
Postal code
5615783134
Phone
+98 45 3352 2247
Email
s.bohlooli@pharmacy.arums.ac.ir
Grant name
Grant code / Reference number
Is the source of funding the same sponsor organization/entity?
Yes
Title of funding source
Ardabil University of Medical Sciences
Proportion provided by this source
100
Public or private sector
Public
Domestic or foreign origin
Domestic
Category of foreign source of funding
empty
Country of origin
Type of organization providing the funding
Academic

Person responsible for general inquiries

Contact
Name of organization / entity
Ardabil University of Medical Sciences
Full name of responsible person
Elnaz Eskandar pour
Position
resident
Latest degree
Medical doctor
Other areas of specialty/work
Pediatrics
Street address
Moallem Street
City
Ardabil
Province
Ardabil
Postal code
5615783134
Phone
+98 45 3325 2251
Email
e.eskandarpour@arums.ac.ir

Person responsible for scientific inquiries

Contact
Name of organization / entity
Ardabil University of Medical Sciences
Full name of responsible person
Elnaz Eskandar pour
Position
resident
Latest degree
Medical doctor
Other areas of specialty/work
Pediatrics
Street address
Moallem Street
City
Ardabil
Province
Ardabil
Postal code
۵۶۱۳۶۴۳۱۹۷
Phone
+98 45 3325 2251
Email
e.eskandarpour@arums.ac.ir

Person responsible for updating data

Contact
Name of organization / entity
Ardabil University of Medical Sciences
Full name of responsible person
Elnaz Eskandar pour
Position
Resident
Latest degree
Medical doctor
Other areas of specialty/work
Pediatrics
Street address
Moallem Street
City
Ardabil
Province
Ardabil
Postal code
۵۶۱۳۶۴۳۱۹۷
Phone
+98 45 3325 2251
Email
e.eskandarpour@arums.ac.ir

Sharing plan

Deidentified Individual Participant Data Set (IPD)
Undecided - It is not yet known if there will be a plan to make this available
Study Protocol
Undecided - It is not yet known if there will be a plan to make this available
Statistical Analysis Plan
Not applicable
Informed Consent Form
Undecided - It is not yet known if there will be a plan to make this available
Clinical Study Report
Undecided - It is not yet known if there will be a plan to make this available
Analytic Code
Not applicable
Data Dictionary
Not applicable
Loading...