No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 45
Sex
Female
Study type
Observational
Participants needed
400 (estimated)
Sponsor
University of Kansas Medical Center · Other
Who this trial is looking for
This trial is looking for pregnant women who have used GLP-1RA medications for weight loss before pregnancy. Participants will fill out questionnaires about their experiences with food and medication during and after their pregnancy.
Are You a Good Fit for This Trial?
You may be able to join if
I am an adult woman
I am less than 20 weeks pregnant at my first visit
I speak English
You may not be able to join if
I am under 18 years old at my first visit
I have type 2 diabetes
I have had bariatric surgery
I am pregnant with more than one baby
I cannot consent for myself
I cannot read and speak English
I am incarcerated
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 a…
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.
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria:
* Adult women
* Less than or equal to 20 weeks gestation at first visit
* English speaking
Exclusion Criteria:
* \<18 years at time of initial visit
* Type 2 diabetes
* History of bariatric surgery
* Multiple gestation
* Cannot consent for themselves
* Cannot read and speak En…
Inclusion Criteria:
* Adult women
* Less than or equal to 20 weeks gestation at first visit
* English speaking
Exclusion Criteria:
* \<18 years at time of initial visit
* Type 2 diabetes
* History of bariatric surgery
* Multiple gestation
* Cannot consent for themselves
* Cannot read and speak English
* Incarcerated
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