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临床试验/NCT04808206
NCT04808206进行中(未招募)不适用

A Multicentric Prospective Registry of Laparoscopic Bariatric Surgery Using Stapling Devices: Observation of Safety and Clinical Efficacy

Duomed3 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2022年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
Duomed
入组人数
150
试验地点
3
主要终点
Safety of laparoscopic bariatric surgery using stapling devices (easyEndoTM Universal Linear Cutting Stapler and reloads - Ezisurg Medical)

研究概览

简要总结

The purpose of this observational registry is to evaluate the safety and the clinical efficacy of laparoscopic bariatric surgery using stapling devices (easyEndoTM Universal Linear Cutting Stapler and reloads from Ezisurg Medical). The goal of the study will be achieved by reporting peri- and postoperative complications and the clinical outcome after surgery in a prospectively maintained database.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient ≥ 18 years of age at registry entry
  • Patient and investigator signed and dated the informed consent form prior to the index-procedure.
  • Patient has a BMI ≥ 35 kg/m2, with one or more related co-morbidities.
  • Patient has a BMI ≥ 40 kg/m
  • Patient is eligible for laparoscopic bariatric surgery.

排除标准

  • Patient is unable/unwilling to provide informed consent.
  • Patient has a history of bariatric surgery.
  • Patient is unable to comply with the registry protocol or the proposed follow-up visits.
  • Patient has a contra-indication for laparoscopic bariatric surgery.

结局指标

主要结局

Safety of laparoscopic bariatric surgery using stapling devices (easyEndoTM Universal Linear Cutting Stapler and reloads - Ezisurg Medical)

时间窗: Follow-up 4: 24 months after the procedure

Number of re-interventions and number of participants with (serious) adverse events ≥ grade II Clavien-Dindo.

次要结局

  • Clinical efficacy - weight loss(Follow-up 4: 24 months after the procedure)
  • Device performance(At index procedure)
  • Number of participants with a post-operative change of cormorbidities(Follow-up 4: 24 months after the procedure)

研究者

发起方
Duomed
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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