Gestational Weight Gain and Pregnancy Outcomes After GLP-1 Receptor Agonist Discontinuation.
Jacqueline Maya, Deepti Pant, Yiran Fu...
https://pubmed.ncbi.nlm.nih.gov/41284263/Actively Recruiting
Led by University of Kansas Medical Center · Updated on 2026-08-04
400
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are studying pregnant women to understand how using glucagon-like peptide-1 receptor agonists GLP-1RAs for weight loss before pregnancy affects weight gain during pregnancy and pregnancy outcomes. This study compares women who used GLP-1RA medications before conceiving to those who did not use these medications. It aims to provide insights on how stopping GLP-1RA treatment before pregnancy influences maternal and newborn health. The study is observational and does not provide any treatment or intervention. About 400 pregnant women aged 18 to 45 years, who are at or before 20 weeks of pregnancy, will be enrolled. Participants will be divided into two groups based on whether they used GLP-1RA medications within three years before conception. Participants will complete questionnaires at several points during and after pregnancy, including early pregnancy, late pregnancy 32-36 weeks, 6-10 weeks postpartum, and 6 months postpartum. During the study, participants will provide information about their medication history, eating habits, and infant feeding practices through questionnaires. Clinical data about mother and baby will be collected from medical records. The main outcome measured is the amount of weight gained from the start of pregnancy to delivery. Researchers will also compare obstetrical outcomes and eating behaviors between groups. The study will last until April 2028, with multiple assessments over pregnancy and postpartum periods.
CONDITIONS
Gestational Response, Outcomes, and Weight After GLP-1 Use
M
Molly Fain
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University of Kansas Medical Center
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - From enrollment until 6 months postpartum
Participants complete questionnaires during early and late pregnancy, and at 6-10 weeks and 6 months postpartum. Clinical information is collected from medical records to compare outcomes between groups.
Questionnaires at multiple timepoints during and after pregnancy
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Jacqueline Maya, Deepti Pant, Yiran Fu...
https://pubmed.ncbi.nlm.nih.gov/41284263/Duy Do, Tiffany Lee, Samuel K Peasah...
https://pubmed.ncbi.nlm.nih.gov/38787563/University of Kansas Medical Center
Lead Sponsor