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Effect of Obesity, Diabetes and Bariatric Surgery on Pregnancy Outcomes

Investigation and Study of Pregnancy in Overweight or Diabetic Women and the Effect of Bariatric Surgery on Pregnancy Outcomes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05753124
Enrollment
700
Registered
2023-03-03
Start date
2015-05-31
Completion date
2027-10-31
Last updated
2023-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bariatric Surgery Status Complicating Pregnancy, Obesity, Pregnancy Complications, Pregnancy in Diabetic, Pregnancy Related

Keywords

Pregnancy, Gastric sleeve, Gastric bypass, Bariatric surgery, Birth weight, Glucose intolerance

Brief summary

The obesity epidemic is growing worldwide and in the UK this is perpetuated with a third of women classified as overweight/obese in 2020. Many of these woman are of childbearing age and go on to have high risk pregnancies which are often complicated by gestational or pre-existing (type 2 diabetes mellitus (GDM, T2DM). Bariatric surgery is the most successful treatment of sustainable weight loss and is associated with a reduction in rates of GDM, pre-eclampsia, delivery of large babies but increased risk of delivery of small babies and preterm delivery. The aims of the study are to investigate the maternal and fetal/neonatal, biophysical and biochemical, intra-uterine environment and postnatal profile of pregnancies: 1. affected by maternal obesity and/or GDM/T2DM compared to pregnancies with normal maternal body mass index (BMI). 2. with previous maternal bariatric surgery compared to pregnancies without previous bariatric surgery but matched for maternal pre-surgery and early pregnancy BMI.

Detailed description

This is an observational study. The investigators are planning to study pregnant women with normal BMI or overweight (BMI\<30), obesity (BMI ≥30) and glucose disorders (GDM and T2DM). The investigators will also study pregnant women with previous bariatric surgery (gastric band, sleeve gastrectomy or gastric bypass) and compare them with pregnant women of similar pre-surgery and early pregnancy BMI, but no hisotry of weight loss surgery. For all the participants and serially during pregnancy (at 12-14, 20-24, 26-28, 30-32, 35-37 weeks gestation and postnatally (at 6 weeks, 3 months, 12-24 months and 3-7 years of age), the investigators will perform the following investigations: Maternal investigations: Demographics and medical history will be recorded, weight, height, waist to hip ratio and blood pressure will be measured, blood, urine, stool samples and vaginal swabs will be obtained, cervical length (by trans-vaginal ultrasound) will be measured and maternal echocardiography will be performed. Maternal glucose homeostasis will be assessed at 26-28 weeks of gestation, by a full oral glucose tolerance test, HOMA, home glucose monitoring and/ or continuous glucose monitoring (CGM), depending on the group the women belong to. Fetal investigations: Fetal growth and well being will be assessed by 2D, 3D and Doppler ultrasound, fetal echocardiography will be performed. At and following delivery: Maternal blood and urine samples and subcutaneous and omental fat (if Caesarean section is performed) will be obtained, placental tissue will be stored. Neonatal cord blood will be obtained, birthweight (percentiles), anthropometric characteristics will be measured, meconium and urine samples will be obtained and neonatal MRI (to assess body fat distribution) will be arranged. Postnatal follow up visits for the mother and the infant (at 6 weeks, 3 months, 12-24 months, 3-7 years old) will be arranged and maternal and infant blood and urine samples will be requested and obtained.

Interventions

OTHERObservational

This is an observational study

Sponsors

Chelsea and Westminster NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women with normal size (BMI \<30) * Pregnant women with obesity (BMI ≥30) * Pregnant women with glucose disorders * Pregnant women with previous bariatric surgery

Exclusion criteria

* Pregnant women less than 18 years of age * Pregnant women with twins/triplets

Design outcomes

Primary

MeasureTime frameDescription
Birth weight (in percentiles)At the time of birthBirthweight percentiles will be compared in the groups studied

Secondary

MeasureTime frameDescription
Reported pregnancy complicationsDuring pregnancy and up until the birth of the babyCompare the percentage of women that develop pre-eclampsia or other complications in the groups studied
Reported labour outcomesAt birthThe percentage of women who deliver by instrumental deliveries or Caesarean section, in the groups studied
Maternal and infant weight (in kg) and height (in cm)Following the birth: 6 weeks, 3 months, 12-24 months and 3-7 yearsWeight and height will be combined to report BMI in kg/m\^2, in the groups of women studied
Maternal and infant blood pressure (in mmHg)Following the birth: 6 weeks, 3 months, 12-24 months and 3-7 yearsCompare the maternal and infant biophysical profile in the groups of women studied
Maternal and infant blood and urine samplesFollowing the birth: 6 weeks, 3 months, 12-24 months and 3-7 yearsCompare the maternal and infant metabolic profile in the groups of women studied

Countries

United Kingdom

Contacts

Primary ContactDAMON FOSTER
damon.foster2@nhs.net
Backup ContactDORIS DABY
doris.daby1@nhs.net

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026