Does Weight-Loss surgery change how babies grow in the womb?
NCT ID NCT07877233
First seen Oct 16, 2026 · Last updated Oct 16, 2026
Summary
Researchers are studying how pregnancy after bariatric surgery affects the nutritional status of mothers and their babies. The study follows pregnant women who had gastric bypass or sleeve gastrectomy and compares them with pregnant women who did not have surgery. Participants give blood and urine samples, answer diet questions, and use a glucose monitor. The team tracks vitamin levels, weight gain, pregnancy complications, and newborn growth to learn whether surgery changes nutritional needs during pregnancy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If researchers find that pregnancy after bariatric surgery raises the risk of vitamin deficiencies or complications, the results could shape nutritional guidelines and monitoring for these women. It could also help doctors advise on the best timing for pregnancy after surgery.
- What could go wrong
- This is an observational study, so it can show links but cannot prove that surgery causes any differences. Findings may not apply to women outside Norway or to those with different surgical histories, and results may reflect other lifestyle or health factors.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 210 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Nord Trøndelag Hospital Trust Namsos and Levanger Hospital St Olavs University Hospital Møre and Romsdal Hospital Trust, Ålesund Hospital
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * pregnant * sufficient understanding of the Norwegian or Scandinavian language * written informed consent Exclusion Criteria: * multiple gestations, * pre-pregnancy BMI \< 18.5 kg/m2 * insulin treated diabetes mellitus * termination of pregnancy before 14 weeks (spontaneously or induced) * anorexia * bullemia
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Namsos Hospital
RECRUITINGNamsos, Trøndelag, 7800, Norway
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St Olavs University Hospital
RECRUITINGTrondheim, Trøndelag, 7800, Norway
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Ålesund Hospital
RECRUITINGÅlesund, Møre og Romsdal, Norway
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Other studies related to the condition(s) this trial covers.
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