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CTRI Number  CTRI/2023/05/052339 [Registered on: 08/05/2023] Trial Registered Prospectively
Last Modified On: 03/05/2023
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Other 
Public Title of Study   A study to compare the efficacy of Injection Carbetocin with Injection Oxytocin to prevent postpartum haemorrhage 
Scientific Title of Study   A comparative study of Injection Carbetocin with Injection Oxytocin for the prevention of postpartum haemorrhage. 
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Shreya Dipak Mehta 
Designation  Resident doctor 
Affiliation  GMERS MEDICAL COLLEGE AND HOSPITAL, GOTRI VADODARA 
Address  GMERS medical college campus, Department of OBGYN First floor

Vadodara
GUJARAT
390021
India 
Phone  7567598864  
Fax    
Email  mehtashreya8236@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr AshishKumar N Shah 
Designation  Head of the department 
Affiliation  GMERS MEDICAL COLLEGE AND HOSPITAL, GOTRI VADODARA 
Address  Department of OBGYN GMERS Medical college and Hospital Gotri Vadodara

Vadodara
GUJARAT
390021
India 
Phone  8849450012  
Fax    
Email  Drashishshah2001@yahoo.com  
 
Details of Contact Person
Public Query
 
Name  Dr Shreya Dipak Mehta 
Designation  Resident doctor 
Affiliation  GMERS MEDICAL COLLEGE AND HOSPITAL, GOTRI VADODARA 
Address  GMERS medical college campus, Dept of OBGYN, First floor

Vadodara
GUJARAT
390021
India 
Phone  7567598864  
Fax    
Email  mehtashreya8236@gmail.com  
 
Source of Monetary or Material Support  
GMERS hospital Gotri Vadodara 
 
Primary Sponsor  
Name  GMERS MEDICAL COLLEGE AND HOSPITAL 
Address  GMERS MEDICAL COLLEGE AND HOSPITAL GOTRI VADODARA 390021 
Type of Sponsor  Government medical college 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Shreya Dipak Mehta  GMERS MEDICAL COLLEGE AND HOSPITAL  Labor room, first floor GMERS Hospital Gotri VADODARA 390021
Vadodara
GUJARAT 
7567598864

mehtashreya8236@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
IHEC GMERS medical college and hospital  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Healthy Human Volunteers  Women in labor undergoing birth process 
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Injection Carbetocin  Efficacy in the prevention of post partum hemorrhage Dose: 100 mcg IV single dose after delivery of placenta  
Comparator Agent  Injection Oxytocin  Efficacy in the prevention of post partum haemorrhage Dose: 10 IU IM single dose after delivery of placenta  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  45.00 Year(s)
Gender  Female 
Details  1) Primigravida
2) Multigravida
3) Singleton pregnancy
4) Multiple pregnancy
5) Previous cesarean section
6) Currently undergoing normal, instrumental delivery or C-section. 
 
ExclusionCriteria 
Details  1) High blood pressure (eclampsia, pre eclampsia, gestational hypertension, chronic hypertension)
2) Cardiovascular problems
3) Known contraindication to Inj Carbetocin or Inj Oxytocin 
 
Method of Generating Random Sequence   Coin toss, Lottery, toss of dice, shuffling cards etc 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
Number of patients developing PPH after Inj Carbetocin and number of patients developing PPH after Inj Oxyotcin  First 24 hours after delivery 
 
Secondary Outcome  
Outcome  TimePoints 
Number of patients developing side effects of Injection Carbetocin and Injection Oxytocin  First 24 hours after delivery 
 
Target Sample Size   Total Sample Size="80"
Sample Size from India="80" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   10/05/2023 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   None yet 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Introduction: 

Postpartum haemorrhage is defined as any blood loss >500 ml in vaginal delivery or >1000ml in c section. It can also be defined as a fall in Hematocrit by >10%

Uterine atony, till date remains the major cause of PPH. 

 

As a prevention for this, oxytocics have been used as uterotonics after the delivery of the baby.

WHO recommends active management of third stage of labor (AMTSL) which has four components: 1) Injecting a uterotonic to the mother after baby delivery 2) Delayed cord clamping 3) Deliver the placenta by controlled cord traction 4) Intermittent assessment of uterine tone.

 

WHO in its newer recommendations has included Inj Carbetocin as an oxytocic for AMTSL.

Carbetocin works as an oxytocic, anti hemorrhagic and a uterotonic drug. Carbetocin has a much longer lasting effect as compared to oxytocin necessitating a single dose administration.

 

The aim of the study is to throw some more light on the results of Carbetocin administration for prevention of PPH as not many studies have been done in India compared to he number of studies done abroad.

 

AIMS AND OBJECTIVES:

PRIMARY OBJECTIVE:

To compare the efficacy of Injection Carbetocin with Injection Oxytocin for the prevention of PPH.

 

SECONDARY OBJECTIVE:

To compare the safety of Injection Carbetocin with Injection Oxytocin.

 

METHODOLOGY:

 

TYPE OF STUDY:

A RANDOMISED CONTROL TRIAL

 

STUDY SETTING:

Labor room and emergency OT at department of obstetrics and gynaecology at GMERS medical college and general hospital Gotri Vadodara. Patients presenting to the labor room of GMERS hospital Gotri Vadodara in active labor and delivering by either Vaginal delivery or c section in a period of 1 year beginning from 1/3/2023 to 1/3/2024

 

STUDY PERIOD: 

1 year

 

STUDY PROCESS: A randomised trial will be conducted in two groups with a total of 80 patients, 40 in each group. 40 women will receive Inj Carbetocin 100 mcg IV single dose after the delivery of the placenta and 40 women will receive Inj Oxytocin 10IU IM after the delivery of the placenta. 

 

A comparison will be made between the incidence of PPH between women receiving Inj Carbetocin and women receiving Inj Oxytocin by measuring the amount of blood loss (>500 ml for vaginal deliveries and >1000ml in c sections) or by a decrease in hematocrit by>10

 

A comparison will be made between the incidence of side effects in women receiving Inj Carbetocin and women receiving Inj Oxytocin.

 

Individual side effects of each drug are:

Inj Carbetocin:

Nausea, vomiting

Abdominal pain

Increased body temperature

Trembling

Weakness

Dizziness

Chills and sweating 

Chest pain

Tachycardia

Respiratory distress

 

Inj Oxytocin:

Nausea , vomiting

Increased blood pressure

Cardiac arrhythmia 

Anaphylaxis 

Water retention

 

 

INCLUSION CRITERIA: 

1.Primigravida

2.Multigravida

3.Singleton pregnancy

4.Multiple pregnancy

5.Previous cesarean section

6.Currently undergoing normal, instrumental, C-section.

 

 

EXCLUSION CRITERIA: 

1.High blood pressure(eclampsia, pre eclampsia, gestational hypertension, chronic hypertension)

2.Cardiovascular problems

3. Known contraindications to any of the drugs. 

 

SAMPLE SIZE AND SAMPLING METHOD

 

Sample size: 80 

Formula: n0=zx P(1-p) /e2

                      N= n0 x N /n0 + (N+1) 

               n  = sample size of known population

               n0= proportion of unknown population

               N = known population size

 

Type of study: Randomised control trial

Sampling method: Simple random sampling

 

OUTCOME MEASURES: 

1.        Number of patients developing pph after Inj Carbetocin and after Inj Oxytocin. PPH will be identified by the approximate blood loss >500ml after vaginal delivery and >1000 ml after c section or a fall in hematocrit by >10%

2.        Number of patients developing side effects ( as iterated above) of Inj Carbetocin and Inj Oxytocin.

 
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