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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: IRCT
Last refreshed on: 22 February 2018
Main ID:  IRCT2016120330347N1
Date of registration: 2016-12-03
Prospective Registration: No
Primary sponsor: Isfahn University of Medical Sciences
Public title: Comparing the effect of Ranitidin and Pantoprazole on Mg level
Scientific title: Comparing the effect of Ranitidin and Pantoprazole on PICU patients in Imam hossein hospital
Date of first enrolment: 2016-08-17
Target sample size: 70
Recruitment status: Complete
URL:  http://en.irct.ir/trial/24139
Study type:  interventional
Study design:  Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention.  
Phase:  N/A
Countries of recruitment
Iran (Islamic Republic of)
Contacts
Name: Elahe Mansouri   
Address:  Isfahn University of Medical Sciences,Hezargarib street, Isfehan Isfehan Iran (Islamic Republic of)
Telephone: +98 31 3450 1914
Email: Kosar.mansouri@gmail.com
Affiliation:  Isfahn University of Medical Sciences
Name: Dr. Mohammad Reza Habibzade   
Address:  Isfahn University of Medical Sciences, Imam khomeini street, lmam hossein hospital Isfehan Iran (Islamic Republic of)
Telephone: +98 31 3450 1914
Email: habibzadeh@med.mui.ac.ir
Affiliation:  Isfahn University of Medical Sciences
Key inclusion & exclusion criteria
Inclusion criteria: Inclusion: age from 2 months to 15 years old children admited in PICU; consent to participate in the study.
Exclusion criteria: discharging before the end of the study; any condition that need to change the dose of Ranitidin or Pantoprazole for patients e.g GI bleeding.

Exclusion criteria:

Age minimum: 2 months
Age maximum: 15 years
Gender: Both
Health Condition(s) or Problem(s) studied
Magnesium deficiency.
Intervention(s)
Ranitidin, IV, 1 mg/ kg, BID, till end of the study
Pantoprazol, IV, BID,1 mg / kg, till end of the study
Intervention 1: Ranitidin, IV, 1 mg/ kg, BID, till end of the study. Intervention 2: Pantoprazol, IV, BID,1 mg / kg, till end of the study.
Treatment - Drugs
Primary Outcome(s)
Magnesium level. Timepoint: Daily since 7 days. Method of measurement: Labratory kit.
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
Isfahn University of Medical Sciences
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
Isfahn University of Medical Sciences
Results
Results available:
Date Posted:
Date Completed:
URL:
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