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临床试验/NCT03765827
NCT03765827已完成3 期

Effect of the Application of Vitamin E Ointment, Over Staple Lines and Anastomosis in Roux-en-Y Gastric Bypass, on Postoperative Pain

Hospital General Universitario Elche1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2018年12月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
140
试验地点
1
主要终点
Postoperative pain

研究概览

简要总结

Patients will be randomized into 2 groups:

  • Vit E group: Vitamin E ointment will be applied over staple lines and anastomoses
  • Control group: Vitamin E will not be applied

Postoperative pain will be assessed 24 hours after surgery.

详细描述

Patients will be randomized into 2 groups:

  • Vit E group: Vitamin E acetate ointment will be applied over staple lines and anastomoses in Roux-en-Y gastric bypass.
  • Control group: Vitamin E will not be applied

Postoperative pain will be assessed 24 hours after surgery, by means of visuala analogic scale (ranging from 0 to 100mm).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

盲法说明

The patient and the epidemiology nurse will not know the treatgment assigned.

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

  • BMI >40 Kg/m2 or >35 Kg/m2 associated to obesity-related comorbidities
  • Patients undergoing Roux-en-Y gastric bypass as bariatric procedure
  • Patients accepting to participate in the study and signing and Informed Consent form

排除标准

  • Patients undergoing other bariatric techniques
  • Patients undergoing Roux-en-Y gastric bypass as revisional procedure

研究组 & 干预措施

Vitamin E acetate

Experimental

Vitamin E acetate ointment will be applied over the staple lines and anastomoses in Roux-en-Y gastric bypass

干预措施: Vitamine E Acetate (Drug)

Control group

Sham Comparator

No ointment will be applied

干预措施: No application of vitamin E acetate (Drug)

结局指标

主要结局

Postoperative pain

时间窗: 24 hours after surgery

Postoperative pain will be assessed by means of a Visual Analogic Scale, ranging from 0 (absence of pain) to100mm (unbearable pain)

次要结局

未报告次要终点

研究者

发起方
Hospital General Universitario Elche
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jaime Ruiz-Tovar, MD, PhD

Department of Surgery

Hospital General Universitario Elche

研究点 (1)

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