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临床试验/NCT04219852
NCT04219852已完成不适用

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

CHU de Reims1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年9月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
CHU de Reims
入组人数
100
试验地点
1
主要终点
contraception method

研究概览

简要总结

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.

详细描述

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

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women between 18 and 50 years old
  • Followed at Reims University Hospital after bariatric surgery
  • Pre-menopausal status
  • Accepting to participate in the study

排除标准

  • Women less than 18 or more than 50 years old
  • Women with postmenopausal status
  • Women refusing to participate

结局指标

主要结局

contraception method

时间窗: Day 0

Presence of contraception during the postoperative 3 months consultation

次要结局

未报告次要终点

研究者

发起方
CHU de Reims
申办方类型
Other
责任方
Sponsor

研究点 (1)

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