Protocol summary

Study aim
Evaluation of Vancomycin Pharmacokinetics with Two Different Regimens in Patients with Augmented Renal Clearance
Design
Randomized clinical trial with parallel groups on 56 patients. Block randomization method will be used trough online website.
Settings and conduct
This study will be conducted in the Loghman Hakim hospital, Tehran. Patients with augmented renal clearance will be allocated into two groups randomly and vancomycin will be administered every 8 hours or every 12 hours. Finally, blood samples will be taken to measure peak and trough levels of vancomycin.
Participants/Inclusion and exclusion criteria
In this study, patients who needs vancomycin empirically or according to the culture will be included. These patients are over 18 years old and have augmented renal clearance (ARC) score between 7 and 10 or augmented renal clearance in trauma intensive care (ARCTIC) score over than 6. Patients with creatinine level lower than 1.5 mg/dL will be excluded. After initiation of intervention, the clearance of creatinine will be measured with collection of eight hours urine and patients with clearance of creatinine lower than 130 mL/minute will be excluded.
Intervention groups
In the first group, patients will be received intravenous vancomycin manufactured by Exir company at dose of 15 to 20 mg/kg every 12 hours. In the second group, patients will be received intravenous vancomycin manufactured by Exir pharmaceutical company at dose of 15 to 20 mg/kg every 8 hours. The infusion rate of vancomycin is 1000 mg per hour. One hour after ending the infusion of forth dose, blood sample will be taken to measure the peak level of vancomycin. Then, 30 minutes before administration of fifth dose blood sample will be taken to measure the trough level of vancomycin.
Main outcome variables
Ratio of patients who achieves Area under the curve (AUC)/Minimum inhibitory concentration (MIC) over 400.

General information

Reason for update
Acronym
IRCT registration information
IRCT registration number: IRCT20180802040665N1
Registration date: 2021-02-20, 1399/12/02
Registration timing: prospective

Last update: 2021-02-20, 1399/12/02
Update count: 0
Registration date
2021-02-20, 1399/12/02
Registrant information
Name
Ali Saffaei
Name of organization / entity
Country
Iran (Islamic Republic of)
Phone
+98 21 7780 1199
Email address
saffaei@sbmu.ac.ir
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2021-04-04, 1400/01/15
Expected recruitment end date
2021-10-07, 1400/07/15
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
Evaluation of vancomycin pharmacokinetics with two different regimens in patients with augmented renal clearance
Public title
Evaluation of vancomycin pharmacokinetics in patients with augmented renal clearance
Purpose
Treatment
Inclusion/Exclusion criteria
Inclusion criteria:
Age over 18 years old Need of vancomycin therapy with empirical approach or according to the culture Augmented renal clearance (ARC) score between 7 and 10 Augmented renal clearance in trauma intensive (ARCTIC) score over than 6 Signing the informed consent form
Exclusion criteria:
Blood creatinine level lower than 1.5 mg/dL Pregnant or breastfeeding patients Patients with history of vancomycin hypersensitivity Patients with history of vancomycin taking in the current course of hospitalization
Age
From 18 years old
Gender
Both
Phase
2-3
Groups that have been masked
No information
Sample size
Target sample size: 56
Randomization (investigator's opinion)
Randomized
Randomization description
Block randomization method was used in this study. 14 blocks including 4 patients generated with online website. In each block, two patients will be assigned to group A (every 12 hours) and two patients will be assigned to group B (every 8 hours).
Blinding (investigator's opinion)
Not blinded
Blinding description
Placebo
Not used
Assignment
Parallel
Other design features

Secondary Ids

empty

Ethics committees

1

Ethics committee
Name of ethics committee
Vice-Chancellor in Research Affairs - Shahid Beheshti University of Medical Sciences
Street address
3 rd floor, School of Medicine, Evin St, Shahid Chamran Highway
City
Tehran
Province
Tehran
Postal code
1983963113
Approval date
2021-02-14, 1399/11/26
Ethics committee reference number
IR.SBMU.PHARMACY.REC.1399.356

Health conditions studied

1

Description of health condition studied
Augmented renal clearance
ICD-10 code
R94.4
ICD-10 code description
Abnormal results of kidney function studies

Primary outcomes

1

Description
Ratio of patients with Area under the curve (AUC)/Minimum inhibitory concentration (MIC) over 400
Timepoint
Three days after initiation of intervention
Method of measurement
High performance liquid chromatography

Secondary outcomes

1

Description
Blood trough level of vancomycin
Timepoint
Three days after initiation of intervention
Method of measurement
High performance liquid chromatography

2

Description
Getting acute kidney injury
Timepoint
Seven days after initiation of intervention
Method of measurement
Measurement of creatinine blood level

Intervention groups

1

Description
Intervention group: patients will be received intravenous vancomycin manufactured by Exir pharmaceutical company at dose of 15 to 20 mg/kg every 12 hours. The infusion rate of vancomycin is 1000 mg per hour.
Category
Treatment - Drugs

2

Description
Intervention group: patients will be received intravenous vancomycin manufactured by Exir pharmaceutical company at dose of 15 to 20 mg/kg every 8 hours. The infusion rate of vancomycin is 1000 mg per hour.
Category
Treatment - Drugs

Recruitment centers

1

Recruitment center
Name of recruitment center
Loghman Hakim hospital
Full name of responsible person
Ilad Alavi Darazam
Street address
Loghman Hakim Hospital, Kamali St, Makhsoos St
City
Tehran
Province
Tehran
Postal code
1333635445
Phone
+98 21 5541 9005
Email
ilad13@yahoo.com

Sponsors / Funding sources

1

Sponsor
Name of organization / entity
Shahid Beheshti University of Medical Sciences
Full name of responsible person
Afshin Zarghi
Street address
3 rd floor, School of Medicine, Evin St, Shahid Chamran Highway
City
Tehran
Province
Tehran
Postal code
1983963113
Phone
+98 21 23871
Email
mpd@sbmu.ac.ir
Grant name
Grant code / Reference number
Is the source of funding the same sponsor organization/entity?
Yes
Title of funding source
Shahid Beheshti 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
Shahid Beheshti University of Medical Sciences
Full name of responsible person
Zahra Sahraei
Position
Assistant professor
Latest degree
Specialist
Other areas of specialty/work
Medical Pharmacy
Street address
Valieasr St, Niyayesh Highway, Shahid Beheshti University of Medical Sciences, School of Pharmacy
City
Tehran
Province
Tehran
Postal code
1991953381
Phone
0098218200118
Email
zahra.sahraei@yahoo.com

Person responsible for scientific inquiries

Contact
Name of organization / entity
Shahid Beheshti University of Medical Sciences
Full name of responsible person
Minoosh Shabani
Position
Assistant professor
Latest degree
Specialist
Other areas of specialty/work
Infectious diseases
Street address
Loghman Hakim Hospital, Kamali St, Makhsoos St
City
Tehran
Province
Tehran
Postal code
1991953381
Phone
0098218200118
Email
shabaniminoosh@gmail.com

Person responsible for updating data

Contact
Name of organization / entity
Shahid Beheshti University of Medical Sciences
Full name of responsible person
Ali Saffaei
Position
Clinical Pharmacy Resident
Latest degree
Specialist
Other areas of specialty/work
Medical Pharmacy
Street address
Valieasr St, Niyayesh Highway, Shahid Beheshti University of Medical Sciences, School of Pharmacy
City
Tehran
Province
Tehran
Postal code
1991953381
Phone
+98 21 7780 1199
Fax
Email
Saffaei@sbmu.ac.ir

Sharing plan

Deidentified Individual Participant Data Set (IPD)
Yes - There is 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
Undecided - It is not yet known if there will be a plan to make this available
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
Undecided - It is not yet known if there will be a plan to make this available
Data Dictionary
Undecided - It is not yet known if there will be a plan to make this available
Title and more details about the data/document
All potential data can be shared after blinding
When the data will become available and for how long
Six mounts after results published
To whom data/document is available
Researchers working in academic institutions
Under which criteria data/document could be used
For research purposes and meta analysis
From where data/document is obtainable
Dr. Zahra Sahraei Valieasr St, Niyayesh Highway, Shahid Beheshti University of Medical Sciences, School of Pharmacy, 3rd floor, Department of Clinical Pharmacy Zip Code: 1996835113 Telephone: +982188200209 Email: z.sahraei@sbmu.ac.ir
What processes are involved for a request to access data/document
Official letter to the researchers, then after 7 days, their request will be answered.
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