Clinical Trials Directory

Trials / Completed

CompletedNCT04219852

Contraception and Bariatric Surgery: Evaluation of Contraception and Contraceptive Knowledge of Women Undergoing Bariatric Surgery at the University Hospital of Reims

Status
Completed
Phase
Study type
Observational
Enrollment
100 (actual)
Sponsor
CHU de Reims · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Obesity is a public health phenomenon affecting more than 17% of women in France, and more than 20% of men and women in Champagne-Ardenne. Obese women are more likely to have an unplanned pregnancy, whereas these pregnancies are more at risk than women of normal weight and should be planned or considered after weight loss. These women are also often less well followed in terms of gynecology and especially on contraception. More and more patients are opting for bariatric surgery. However, bariatric surgery is not trivial. Indeed, the important loss of weight expected is at risk of nutritional deficiencies. In addition, a large number of patients are still obese during the months following surgery. This is why pregnancy is theoretically contraindicated within 12 or 18 months postoperatively. Women with bariatric surgery must have been properly informed of these risks so that they can choose a contraceptive method, and that can be adapted to both their risk factors and the surgical technique performed.

Detailed description

The purpose of this study is to describe contraception in obese women who have undergone bariatric surgery in Champagne-Ardenne.

Conditions

Interventions

TypeNameDescription
OTHERdata collectiondata collection

Timeline

Start date
2019-09-10
Primary completion
2020-04-14
Completion
2020-12-31
First posted
2020-01-07
Last updated
2021-03-03

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04219852. Inclusion in this directory is not an endorsement.