跳至主要内容
临床试验/NL-OMON39934
NL-OMON39934已完成不适用

The effect of Roux-en-Y gastric bypass surgery in morbidly obese patients on Pharmacokinetics of (Acetyl)salicylic acid and Omeprazole. - ERY-PAO

Medisch Centrum Haaglanden0 个研究点目标入组 40 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Male or female aged between 18 and 65 years at the time of informed consent.
  • - Written informed consent
  • - Scheduled to undergo RYGB surgery and approved to undergo this procedure according to the inclusion criteria of NOK West (Dutch Obesity Clinic West)
  • - Ability to swallow whole medication tablets

排除标准

  • - Ulceration or leakage of the anastomosis post-surgery, to be determined 6 weeks after the RYGB surgery by the surgeon. This is an exclusion criterium for the second testday, to be determined during the study)
  • - *Redo* patients: patients previously treated for morbid obesity with a gastric sleeve or gastric banding.
  • - Contra-indication to use ASA or omeprazole, e.g. known or suspected allergy
  • - Present use or use of drugs within 4 times the half-life of that drug before the start of the study that might interfere with the metabolism of the investigational drugs (inducers/inhibitors of CYP2C19)
  • - Concurrent disease or increased risk of bleeding which may compromise safety of the administration of the study medication (e.g. Von Willebrands disease) according to the judgement of the investigator.
  • - Gastro-intestinal disorders which may impair drug absorption (e.g. Crohn's disease or previous stomach or bowel surgery) according to the judgement of the investigator.
  • - Treatment with any unlicensed drug during the previous month.

研究者

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