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Efficacy of Metformin in Achieving Glycaemia Goals as Recommended for the Treatment of Gestational Diabetes in Non Obese Women

Primary Purpose

Gestational Diabetes, Metformin, Treatment

Status
Terminated
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Metformin
Rapid acting analog insulin Intermediate acting NPH Insulin
Sponsored by
University Hospital, Strasbourg, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gestational Diabetes

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

Women.

  • Age more than 18 and less than 40 years.
  • Unique spontaneous pregnancy.-BMI less than 30kg/m2 before pregnancy.
  • 24 to 30 weeks of amenorrhea or 22 to 28 weeks of gestation.
  • Gestational diabetes.
  • Social Security affiliated subject.- Patient able to understand and signed informed consent.

Exclusion Criteria:

  • Contraindications to metformin.
  • Metformin treatment prior to protocol inclusion.
  • Multiple pregnancies.
  • Diabetes diagnosed prior to pregnancy.
  • High blood pressure prior to pregnancy.
  • Pregnancy hepatic complication
  • High blood pressure prior to study inclusion.
  • Pre or eclampsia.- Premature membranes rupture.

Sites / Locations

  • Hôpitaux Civils de Colmar
  • CHU Dijon,
  • Centre hospitalier de Mulhouse
  • CHU de Reims
  • Hôpitaux Universitaires de Strasbourg

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

treatment by Metformin plus insulin if needed

treatment by insulin

Arm Description

Metformin: from 500 mg 2 time per day to 2500 mg per day; with increment of 500 mg every 5 days until abstention of

Insulin therapy:If post meal (2 hours after meal) glycaemia is > to 120 mg/dl introduce Insulin rapid acting analog (Humalog*, Novorapid*) before the meal concerned and according to the weight. If weight is < 80 kg: breakfast 5U, lunch time 3U, and dinner 4U. If weight is > 80 kg :breakast 6U, lunch time 4U, dinner 5U.If post meal glycaemia stay over 120 mg/dl but lower than130 mg/dl: do 1 U more.If post meal glycaemia stay over 140 mg/dl : do 2 UI moreIf fasting glycaemia is over 95 mg/dl : introduce NPH Insulin (Umuline NPH*, insulatard*) before sleeping : 5U if weight is < 80 kg - 6U if weight is > 80 kgIf fasting glycaemia stay over 95 mg/dl increase NPH Insulin for 1 U and for 2 U if fasting glycaemia is over 110 mg/dl.

Outcomes

Primary Outcome Measures

Efficacy of metformin in treatment of gestational diabetes based on capillary glycaemia with an objective of less than 6 measures out of range

Secondary Outcome Measures

Full Information

First Posted
December 19, 2012
Last Updated
August 24, 2018
Sponsor
University Hospital, Strasbourg, France
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1. Study Identification

Unique Protocol Identification Number
NCT01756105
Brief Title
Efficacy of Metformin in Achieving Glycaemia Goals as Recommended for the Treatment of Gestational Diabetes in Non Obese Women
Official Title
Gestational Diabetes in Non Obese Women and Metformine
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Terminated
Study Start Date
June 2012 (Actual)
Primary Completion Date
February 2018 (Actual)
Study Completion Date
June 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Strasbourg, France

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Gestational diabetes (GD) is defined by a hyperglycemia discovered during pregnancy, leading to fetal and maternal complications which may be prevented by reaching very strict glycaemia targets. Prevalence depends on patient's ethnic group and is about 6 to 14%. This prevalence is increasing due to increased GD risk factors (obesity, pregnancy over 35) and also because criteria of screening have been strengthened after the results of last studies. Usual treatment is diet and in case of failure insulin therapy with multiple injections which may lead to hypoglycemia and weight gain and is very difficult to manage for patients. Some studies have shown the comparable effect of metformin and insulin in about 50% of GD obese patients. The aim of our study is to evaluate efficacy of metformin, outcomes in mother and fetus and baby of metformin. In case of metformin failure, insulin will be added in order to obtain glycaemia in desired goals.Oxidative stress will be assessed in mother blood, baby umbilical cord blood, baby umbilical cord and placenta in 90 women and the oxidative stress compared between insulin and metformin alone treated patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes, Metformin, Treatment, Oxidative Stress

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
treatment by Metformin plus insulin if needed
Arm Type
Experimental
Arm Description
Metformin: from 500 mg 2 time per day to 2500 mg per day; with increment of 500 mg every 5 days until abstention of
Arm Title
treatment by insulin
Arm Type
Active Comparator
Arm Description
Insulin therapy:If post meal (2 hours after meal) glycaemia is > to 120 mg/dl introduce Insulin rapid acting analog (Humalog*, Novorapid*) before the meal concerned and according to the weight. If weight is < 80 kg: breakfast 5U, lunch time 3U, and dinner 4U. If weight is > 80 kg :breakast 6U, lunch time 4U, dinner 5U.If post meal glycaemia stay over 120 mg/dl but lower than130 mg/dl: do 1 U more.If post meal glycaemia stay over 140 mg/dl : do 2 UI moreIf fasting glycaemia is over 95 mg/dl : introduce NPH Insulin (Umuline NPH*, insulatard*) before sleeping : 5U if weight is < 80 kg - 6U if weight is > 80 kgIf fasting glycaemia stay over 95 mg/dl increase NPH Insulin for 1 U and for 2 U if fasting glycaemia is over 110 mg/dl.
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
Metformin: from 500 mg 2 time per day to 2500 mg per day; with increment of 500 mg every 5 days until abstention of
Intervention Type
Drug
Intervention Name(s)
Rapid acting analog insulin Intermediate acting NPH Insulin
Intervention Description
Insulin therapy:If post meal (2 hours after meal) glycaemia is > to 120 mg/dl introduce Insulin rapid acting analog (Humalog*, Novorapid*) before the meal concerned and according to the weight. If weight is < 80 kg: breakfast 5U, lunch time 3U, and dinner 4U. If weight is > 80 kg :breakast 6U, lunch time 4U, dinner 5U.If post meal glycaemia stay over 120 mg/dl but lower than130 mg/dl: do 1 U more.If post meal glycaemia stay over 140 mg/dl : do 2 UI moreIf fasting glycaemia is over 95 mg/dl : introduce NPH Insulin (Umuline NPH*, insulatard*) before sleeping : 5U if weight is < 80 kg - 6U if weight is > 80 kgIf fasting glycaemia stay over 95 mg/dl increase NPH Insulin for 1 U and for 2 U if fasting glycaemia is over 110 mg/dl.
Primary Outcome Measure Information:
Title
Efficacy of metformin in treatment of gestational diabetes based on capillary glycaemia with an objective of less than 6 measures out of range
Time Frame
After diagnosis of gestational diabetes and until 3 months after delivery; screening made between 22th and 28th week of gestation

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women. Age more than 18 and less than 40 years. Unique spontaneous pregnancy.-BMI less than 30kg/m2 before pregnancy. 24 to 30 weeks of amenorrhea or 22 to 28 weeks of gestation. Gestational diabetes. Social Security affiliated subject.- Patient able to understand and signed informed consent. Exclusion Criteria: Contraindications to metformin. Metformin treatment prior to protocol inclusion. Multiple pregnancies. Diabetes diagnosed prior to pregnancy. High blood pressure prior to pregnancy. Pregnancy hepatic complication High blood pressure prior to study inclusion. Pre or eclampsia.- Premature membranes rupture.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nathalie Jeandidier, MD
Organizational Affiliation
University Hospital, Strasbourg, France
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpitaux Civils de Colmar
City
Colmar
ZIP/Postal Code
68024
Country
France
Facility Name
CHU Dijon,
City
Dijon
ZIP/Postal Code
21030
Country
France
Facility Name
Centre hospitalier de Mulhouse
City
Mulhouse
ZIP/Postal Code
68070
Country
France
Facility Name
CHU de Reims
City
Reims
ZIP/Postal Code
51092
Country
France
Facility Name
Hôpitaux Universitaires de Strasbourg
City
Strasbourg
ZIP/Postal Code
67091
Country
France

12. IPD Sharing Statement

Learn more about this trial

Efficacy of Metformin in Achieving Glycaemia Goals as Recommended for the Treatment of Gestational Diabetes in Non Obese Women

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