DECIDE: A Comparative Effectiveness Trial of Oral Metformin Versus Injectable Insulin for the Treatment of Gestational Diabetes

Status: Recruiting
Location: See all (19) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This is a non-inferiority patient-centered and pragmatic comparative-effectiveness pregnancy randomized controlled trial (RCT) with postpartum maternal and child follow-up through 2 years of 1,572 individuals with gestational diabetes mellitus (GDM) randomized to oral metformin versus injectable insulin. This study will determine if metformin is not inferior to insulin in reducing adverse pregnancy outcomes, is comparably safe for exposed individuals and children, and if patient-reported factors, including facilitators of and barriers to use, differ between metformin and insulin. A total of 1,572 pregnant individuals with GDM who need pharmacotherapy will be recruited at 20 U.S. sites using consistent treatment criteria to metformin versus insulin. Participants and their children will be followed through delivery to two years postpartum.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Singleton gestation. Twin reduction to singleton, either spontaneously or therapeutically, is eligible if it occurred before 14 weeks gestational age.

• Age 18 years or older

• Gestational age at randomization between 20 0/7 - 33 6/7 weeks based on project gestational age.

• GDM diagnosis less than or equal to 33 6/7 weeks based on project gestational age.

• Requires medication for glucose control defined as ≥ 30% elevated glucose values (either fasting or postprandial or both) prior to randomization per determination of the provider or documented in the medical record.

• Patient willingness and ability to attend 2-year follow-up visit.

Locations
United States
Alabama
University of Alabama
RECRUITING
Tuscaloosa
California
Cedars Sinai Medical Center
RECRUITING
Los Angeles
University of California San Francisco
RECRUITING
San Francisco
Delaware
Christiana Care
RECRUITING
Newark
Florida
University of South Florida
RECRUITING
Tampa
Massachusetts
Beth Israel Deaconess Medical Center
RECRUITING
Boston
Massachusetts General Hospital
RECRUITING
Boston
Tufts University
RECRUITING
Boston
North Carolina
Wake Forest University
RECRUITING
Winston-salem
New Mexico
University of New Mexico
RECRUITING
Albuquerque
New York
Columbia University Irving Medical Center
RECRUITING
New York
Ohio
The Ohio State University Wexner Medical Center OB/GYN Maternal and Fetal Medicine
RECRUITING
Columbus
Premier Health - Miami Valley Hospital
RECRUITING
Dayton
Pennsylvania
University of Pittsburgh
RECRUITING
Pittsburgh
Rhode Island
Brown University
RECRUITING
Providence
South Carolina
University of South Carolina Greenville
RECRUITING
Greenville
Texas
University of Texas Austin
RECRUITING
Austin
University of Texas Health Science Center
RECRUITING
Houston
Virginia
Eastern Virginia Medical School - Old Dominion University
RECRUITING
Norfolk
Contact Information
Primary
Kartik Venkatesh, MD, PhD
kartik.venkatesh@osumc.edu
614-293-2222
Backup
Anna Bartholomew, MPH, BS, RN
Anna.Bartholomew@osumc.edu
614-685-3229
Time Frame
Start Date: 2024-08-01
Estimated Completion Date: 2030-12
Participants
Target number of participants: 1572
Treatments
Experimental: Metformin
Metformin as either immediate- or extended-release formulations can be utilized, and titrated to a maximum daily dose of 2,500 mg. Participants receiving metformin will have insulin added only if they have not achieved euglycemia for at least 30% of glucose values after generally receiving the maximum daily dose of metformin of 2,500 mg, or in select situations in the setting of participant intolerance due to mild gastrointestinal symptoms. Participants will be asked to continue taking metformin after treatment supplementation with insulin.
Experimental: Insulin
Insulin will be initiated utilizing clinical standards using trimester-specific weight-based dosing criteria, including both basal and prandial insulins for up to a total of 4 daily injections. Consistent with clinical practice, some people may be managed with a single dose of intermediate- or long-acting insulin at night to treat isolated fasting hyperglycemia, while others may require additional treatment of postprandial hyperglycemia with shorter-acting insulin. The sites' insulin formularies include rapid- (Novolog and Humalog), intermediate- (Humulin N, Novolin N, and NPH), and long-acting insulins (Detemir and Lantus).
Related Therapeutic Areas
Sponsors
Collaborators: The George Washington University Biostatistics Center, Patient-Centered Outcomes Research Institute
Leads: Ohio State University

This content was sourced from clinicaltrials.gov