The Impact of Liraglutide on Glucose Tolerance and the Risk of Type 2 Diabetes in Women With Previous Pregnancy-induced Diabetes

NCT01795248 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2020-11-04

No results posted yet for this study

Summary

It is well-known that women with previous gestational diabetes mellitus are in risk of developing type 2 diabetes later in life; approximately half of the women develop overt type 2 diabetes within the first 10 years after pregnancy. Knowing this, we want to examine the effect of the type 2 diabetes medicine, liraglutide (Victoza), in women with previous gestational diabetes with the aim of reducing the risk of developing type 2 diabetes.

Conditions

  • Gestational Diabetes Mellitus

Interventions

DRUG

Liraglutide

1.8 mg liraglutide

DRUG

Placebo

Liraglutide without the GLP-1 analogue

Sponsors & Collaborators

  • Novo Nordisk A/S

    collaborator INDUSTRY
  • Rigshospitalet, Denmark

    collaborator OTHER
  • Hvidovre University Hospital

    collaborator OTHER
  • Herlev Hospital

    collaborator OTHER
  • Hillerod Hospital, Denmark

    collaborator OTHER
  • University of Copenhagen

    collaborator OTHER
  • The Novo Nordisk Foundation Center for Basic Metabolic Research

    collaborator OTHER
  • Aarhus University Hospital

    collaborator OTHER
  • Tina Vilsboll

    lead OTHER

Principal Investigators

  • Tina Vilsbøll, MD, DMSc · University Hospital Gentofte

  • Signe Foghsgaard, MD, PhD · University Hospital Gentofte

  • Emilie Skytte Andersen, MD, PhD-student · Steno Diabetes Center Copenhagen

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-07-31
Primary Completion
2019-09-30
Completion
2020-09-30

Countries

  • Denmark

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01795248 on ClinicalTrials.gov