Metformin for Prevention Gestational Diabetes in Pregnant Women With Polycystic Ovarian Syndrome (MGDPCOS)
Primary Purpose
Polycystic Ovary Syndrome, Diabetes, Gestational
Status
Unknown status
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
metformin
placebo (folic acid )
Sponsored by
About this trial
This is an interventional prevention trial for Polycystic Ovary Syndrome focused on measuring Diabetes Mellitus, Pregnancy
Eligibility Criteria
Inclusion Criteria:
- All women had confirmed diagnosis of PCOS before pregnancy according to revised 2003 Rotterdam criteria.
- Age more than 20 and more than 40 years.
- BMI ranging from (25_35 )
- Written and signed informed consent is given from the patient to participate in the study.
Exclusion Criteria:
- Women with pre-gestational diabetes mellitus confirmed by 2hrs OGTT.
- Patients who take metformin in the first 12 wk of pregnancy.
- Patients who are unwilling to participate in the study.
Sites / Locations
- Ain Shams maternity hospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Metformin group
control group
Arm Description
40 women will receive metformin in dose of 1500 mg per day orally (500 mg every 8 hrs in the middle of meal) starting from 12th week of gestation till delivery.
40 women will receive placebo which will be folic acid 500 micro gram which looks like metformin tablet.
Outcomes
Primary Outcome Measures
Number of participants with gestational diabetes by measuring plasma glucose levels ( mg / dl ).
Diagnosis of GDM when these values are met or exceed fasting plasma glucose level (92 mg/dl).1hr level is (180 mg/dl) and 2hrs level is (153 mg/dl).
Secondary Outcome Measures
Fetal adverse effects
Recorded in Case Record Form
Maternal adverse effects
Recorded in Case Record Form
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02802215
Brief Title
Metformin for Prevention Gestational Diabetes in Pregnant Women With Polycystic Ovarian Syndrome
Acronym
MGDPCOS
Official Title
Metformin for Prevention of Gestational Diabetes in Pregnant Women With Polycystic Ovarian Syndrome: Randomized Controlled Trial (RCT )
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
August 2016 (Anticipated)
Study Completion Date
September 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Randomized, placebo controlled clinical trial that evaluate the role of taking metformin therapy during pregnancy in women with polycystic ovarian syndrome(PCOS) in reducing the development of gestational diabetes(GDM) and improving pregnancy outcomes.
Detailed Description
The study will include a total of 80 pregnant women who fulfill the inclusion and exclusion criteria. Participants will be distributed into two groups :
Group A: Active one (40 women) will receive metformin in a dose of 1500mg per day (500mg every 8hrs in the middle of meal), starting from 12th week of gestation till delivery.
Group B: control group (40 women) will receive placebo which will be folic acid 500 micro gram which looks like metformin tablet.
80 opaque envelope will be numbered serially from 1-80, in each envelope paper containing the group to which the participants will be allocated according to randomization table .The envelopes will be put in one box and when the first patient arrives the first envelope will be open and the patient will be allocated according to the paper inside.
Detection of glucose intolerance will be done using oral glucose tolerance test (OGTT), which based on 75 gm to exclude any case of pre-gestational DM. BMI and blood pressure will be also assessed for all cases at entry of the study.
Follow up of all cases in antenatal care clinic, with clinical assessment including weight gain, blood pressure, urine examination for proteinuria and fetal well being tests.
Detection of development of GDM or even glucose intolerance will be by using (OGTT), which based on 75 gm glucose between 24th-28th wk and also can be repeated between 32th- 34th wk of pregnancy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome, Diabetes, Gestational
Keywords
Diabetes Mellitus, Pregnancy
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Metformin group
Arm Type
Active Comparator
Arm Description
40 women will receive metformin in dose of 1500 mg per day orally (500 mg every 8 hrs in the middle of meal) starting from 12th week of gestation till delivery.
Arm Title
control group
Arm Type
Placebo Comparator
Arm Description
40 women will receive placebo which will be folic acid 500 micro gram which looks like metformin tablet.
Intervention Type
Drug
Intervention Name(s)
metformin
Other Intervention Name(s)
cidophage
Intervention Description
Metformin group will receive 1500 mg of metformin per day orally ( 500 mg every 8hrs in the middle of meal) starting from 12th week of gestation till delivery.
Intervention Type
Drug
Intervention Name(s)
placebo (folic acid )
Other Intervention Name(s)
folicap
Intervention Description
500 micro gram of folic acid every 8 hrs
Primary Outcome Measure Information:
Title
Number of participants with gestational diabetes by measuring plasma glucose levels ( mg / dl ).
Description
Diagnosis of GDM when these values are met or exceed fasting plasma glucose level (92 mg/dl).1hr level is (180 mg/dl) and 2hrs level is (153 mg/dl).
Time Frame
24th -28th week gestation
Secondary Outcome Measure Information:
Title
Fetal adverse effects
Description
Recorded in Case Record Form
Time Frame
from 12th week gestation till delivery
Title
Maternal adverse effects
Description
Recorded in Case Record Form
Time Frame
from 12th week gestation till delivery
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All women had confirmed diagnosis of PCOS before pregnancy according to revised 2003 Rotterdam criteria.
Age more than 20 and more than 40 years.
BMI ranging from (25_35 )
Written and signed informed consent is given from the patient to participate in the study.
Exclusion Criteria:
Women with pre-gestational diabetes mellitus confirmed by 2hrs OGTT.
Patients who take metformin in the first 12 wk of pregnancy.
Patients who are unwilling to participate in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ahmed E elbohoty, MD
Email
elbohoty79@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed E elbohoty, MD
Organizational Affiliation
Ain Shams University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Reda k Mokhtar, MD
Organizational Affiliation
Ain Shams University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
mai R ibrahim, MBBCH
Organizational Affiliation
Ain Shams University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ain Shams maternity hospital
City
Cairo
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ahmed E Elbohoty, Ph.D.
12. IPD Sharing Statement
Plan to Share IPD
Yes
Learn more about this trial
Metformin for Prevention Gestational Diabetes in Pregnant Women With Polycystic Ovarian Syndrome
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