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Assessment of the efficacy of hydrogel-based wound dressing containing allantoin and silver nanoparticles in the treatment of second-degree burn wounds: A randomized clinical trial

Protocol summary

Study aim
Determining and comparing the effect of hydrogel-based wound dressing containing allantoin and silver nanoparticles on healing second-degree burns wounds
Design
Two arms parallel-group randomized trials with a control group and blinded participants on 86 patients. The blocking method is used for randomization.
Settings and conduct
This study is performed in the burn department of Imam Reza Hospital. 86 patients with second-degree burns (less than 20% of burns) are randomly assigned into two groups. Group A patients receive hydrogel-based wound dressing containing allantoin and silver nanoparticles and then dry gauze and bandaging, and group B patients receive the usual treatment (a layer of fatty gauze, dry gauze, and then bandaging). Every 48 hours, the secondary dressing is replaced, and the wound is evaluated in terms of infection and the progress of wound healing. Participants in this study are blind to the treatment they receive.
Participants/Inclusion and exclusion criteria
Inclusion criteria: aged between 2 to 60 years; second-degree burn wounds; diagnosed by the relevant physician; burns less than or equal to 20%; burn in upper and lower limbs and anterior trunk; wound examined by plastic and burn surgeon for necrosis and depth of the burn and the burned area is not a candidate for early surgery and the area heals without surgery and with minimal complications. Exclusion criteria: Chemotherapy; Patients taking corticosteroids; Pregnancy; Cancer, cytotoxic drugs, immunosuppressants, diabetes, and renal failure;
Intervention groups
The intervention group consisted of 43 patients who underwent hydrogel-based wound dressing containing allantoin and silver nanoparticles. The control group (43 patients) receive the usual treatment (a layer of fatty gauze, dry gauze, and then bandaging).
Main outcome variables
Duration of complete wound healing

General information

Reason for update
Acronym
IRCT registration information
IRCT registration number: IRCT20210918052511N2
Registration date: 2022-04-06, 1401/01/17
Registration timing: prospective

Last update: 2022-04-06, 1401/01/17
Update count: 0
Registration date
2022-04-06, 1401/01/17
Registrant information
Name
Omid Yazarlu
Name of organization / entity
Country
Iran (Islamic Republic of)
Phone
+98 51 3841 2073
Email address
yazarlouom@mums.ac.ir
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2022-04-20, 1401/01/31
Expected recruitment end date
2022-12-21, 1401/09/30
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
Assessment of the efficacy of hydrogel-based wound dressing containing allantoin and silver nanoparticles in the treatment of second-degree burn wounds: A randomized clinical trial
Public title
Assessment of the efficacy of hydrogel-based wound dressing containing allantoin and silver nanoparticles in the treatment of second-degree burn
Purpose
Treatment
Inclusion/Exclusion criteria
Inclusion criteria:
Patients between the ages of 2 and 60 are eligible to participate. Patients with second-degree burns diagnosed by the relevant physician Patients with burns that are less than or equal to 20% Patient with second-degree burns in upper and lower limbs and anterior trunk The wound is examined by a plastic and burn surgeon for necrosis and the depth of the burn. If the burned area is not a candidate for early surgery and can be healed without surgery and with minimal complications, the patient will be eligible to the study.
Exclusion criteria:
Delayed visit and the presence of obvious wound infection at the first visit by an infectious disease specialist Patients who are receiving chemotherapy Patients taking corticosteroids or cytotoxic medicines Pregnancy Cancer, cytotoxic drugs, immunosuppressants, and the presence of chronic diseases other than diabetes that affect wound healing, such as severe vascular disease, lupus, rheumatoid arthritis, and renal failure Smoking The presence of an underlying disease leads to a defective immune system Diabetic patients Taking drugs that lead to a defective immune system. Burns in the back of the trunk, face, head and perineum
Age
From 2 years old to 60 years old
Gender
Both
Phase
2
Groups that have been masked
  • Participant
Sample size
Target sample size: 86
Randomization (investigator's opinion)
Randomized
Randomization description
Each of the 86 patients would be assigned a number between 1 and 86 which is randomized by using random.org/integers in two columns. ​The numbers of the first column are assigned to group A and the second column is assigned to group B. With a lottery method, each column (A or B) is assigned to the intervention or control groups.
Blinding (investigator's opinion)
Single blinded
Blinding description
Prior to participating in the trial, all patients or their legal representatives sign an informed consent form and are informed that they will be in one of two treatment groups. After that, participants receive the dressing based on how the allocation occurred, and they are unaware of the type of dressing received.
Placebo
Not used
Assignment
Parallel
Other design features

Secondary Ids

empty

Ethics committees

1

Ethics committee
Name of ethics committee
Research ethics committee of school of medicine-Mashhad university of medical sciences
Street address
Azadi squer- campus of Medical University of Mashhad
City
Mashhad
Province
Razavi Khorasan
Postal code
91379-13316
Approval date
2021-12-06, 1400/09/15
Ethics committee reference number
IR.MUMS.MEDICAL.REC.1400.815

Health conditions studied

1

Description of health condition studied
Burn patients
ICD-10 code
T20
ICD-10 code description
Burn and corrosion of head, face, and neck

Primary outcomes

1

Description
Duration of complete wound healing
Timepoint
Every 48 hours
Method of measurement
Based on the clinical observations of an infectious disease specialist and plastic and burn surgeon

Secondary outcomes

1

Description
Wound condition (presence or absence of granulation tissue, bleeding, pain, infection, and other wound complications or healing factors).
Timepoint
Every 48 hours for 2 weeks
Method of measurement
Based on the scores of the variables and presence or absence (yes / no) and based on clinical observations of an infectious disease specialist and subspecialty of plastic surgery and burns

Intervention groups

1

Description
Intervention group: The hydrogel-based wound dressing containing allantoin and silver nanoparticles is used for two weeks and this dressing in the treatment of burn wounds accelerates wound healing, reduces the need to change dressings, shortens the duration of hospitalization, reduces scar formation, temperature control, proper air permeability to the wound and reduce pain and earlier removal of the dressing. For wound dressing, the secondary dressing (dry gauze and bandage) is changed every 48 hours and if necessary, the hydrogel dressing is also changed.
Category
Treatment - Devices

2

Description
Control group: includes the conventional treatment (a layer of fatty gauze, dry gauze and then bandaging) for two weeks.
Category
Treatment - Devices

Recruitment centers

1

Recruitment center
Name of recruitment center
Burn department-Imam Reza hospital
Full name of responsible person
Dr. Omid Yazarlou
Street address
Daneshgah street-Burn department-Imam Reza hospital
City
Mashhad
Province
Razavi Khorasan
Postal code
91379-13316
Phone
+98 51 3802 2051
Email
Yazarlouom@mums.ac.ir

Sponsors / Funding sources

1

Sponsor
Name of organization / entity
Mashhad University of Medical Sciences
Full name of responsible person
Dr. Khalil Abnous
Street address
Daneshgah Street- Mashhad University of Medical Sciences
City
Mashhad
Province
Razavi Khorasan
Postal code
13944-91388
Phone
+98 51 3879 5031
Email
AbnousKh@mums.ac.ir
Grant name
Grant code / Reference number
Is the source of funding the same sponsor organization/entity?
No
Title of funding source
Mashhad 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
Mashhad University of Medical Sciences
Full name of responsible person
Dr Omid Yazarlou
Position
Assistant Professor
Latest degree
Subspecialist
Other areas of specialty/work
Plastic & Reconstructive Surgery
Street address
Burn Department of Imam Reza Hospital
City
Mashhad
Province
Razavi Khorasan
Postal code
91379-13316
Phone
+98 51 3802 2051
Email
Yazarlouom@mums.ac.ir

Person responsible for scientific inquiries

Contact
Name of organization / entity
Mashhad University of Medical Sciences
Full name of responsible person
Dr. Omid Yazarlou
Position
Assistant Professor
Latest degree
Subspecialist
Other areas of specialty/work
Plastic & Reconstructive Surgery
Street address
Burn Department of Imam Reza Hospital
City
Mashhad
Province
Razavi Khorasan
Postal code
91379-13316
Phone
+98 51 3802 2051
Email
Yazarlouom@mums.ac.ir

Person responsible for updating data

Contact
Name of organization / entity
Mashhad University of Medical Sciences
Full name of responsible person
Dr Maede Hasanpour
Position
Post-doctoral fellowship
Latest degree
Ph.D.
Other areas of specialty/work
Medical Pharmacy
Street address
Azadi Square - Mashhad School of Pharmacy
City
Mashhad
Province
Razavi Khorasan
Postal code
91775-1365
Phone
+98 51 3180 1251
Email
maede.hasanpour@yahoo.com

Sharing plan

Deidentified Individual Participant Data Set (IPD)
Yes - There is a plan to make this available
Study Protocol
Yes - There is a plan to make this available
Statistical Analysis Plan
Yes - There is a plan to make this available
Informed Consent Form
Yes - There is a plan to make this available
Clinical Study Report
Not applicable
Analytic Code
Not applicable
Data Dictionary
Not applicable
Title and more details about the data/document
Part of the data is related to the main outcome and the secondary outcome can be shared.
When the data will become available and for how long
The access period starts 3 months after the results are published
To whom data/document is available
The data is available to researchers working in academic and scientific institutions as well as people working in the industry.
Under which criteria data/document could be used
Use as a reference
From where data/document is obtainable
Dr. Maede Hasanpour - Faculty of Pharmacy - Room 233 - Phone number 09113145617-maede.hasanpour@yahoo.com
What processes are involved for a request to access data/document
After making a call via email or phone, the desired data will be sent using email or post.
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