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NCT07743567Recruiting

Gestational Response, Outcomes, and Weight After GLP-1 Use

Source: ClinicalTrials.gov · Last updated 4 Aug 2026

Brief summary (registry, in English)

The goal of this observational study is to learn if using GLP-1RA medications for weight loss before pregnancy influences gestational weight gain and pregnancy outcomes. The main aims of the study are to: * Compare gestational weight gain between women with preconception GLP-1RA exposure and those without exposure. * Compare obstetrical outcomes between women with preconception GLP-1RA exposure and those without exposure. Researchers will compare pregnant women with a history of GLP-1RA use to pregnant women who have not used a GLP-1RA to compare differences. Participants will be asked to complete questionnaires at multiple timepoints during and after pregnancy that ask questions about medication history, thoughts and feelings around food, etc.

Status (registry)
Recruiting
Study type
Observational
Enrollment
400 (estimated)
First submitted
30 Jul 2026
Start date
13 Apr 2026
Primary completion date
30 Apr 2028
Lead sponsor
University of Kansas Medical Center
Diseases
Obesity
NCT number
NCT07743567

What you commit to

  • Study type: Observational
  • Planned participants: 400
  • From 13 Apr 2026 to the primary completion date, 30 Apr 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Type 2 diabetes
  • History of bariatric surgery

Age

  • \<18 years at time of initial visit

Other

  • Multiple gestation
  • Cannot consent for themselves
  • Cannot read and speak English
  • Incarcerated

Who the study is looking for

  • Adult women
  • Less than or equal to 20 weeks gestation at first visit
  • English speaking

Age in the registry: 18 years to 45 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Kansas Medical Center
Coordinator of this site? Confirm its status
Kansas CityUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.