跳至主要内容
临床试验/NCT02811926
NCT02811926已完成不适用

Incidence and Risk Factors of Parastomal Bulging in Patients With Ileostomy or Colostomy: a Register-based Study

Rigshospitalet, Denmark0 个研究点目标入组 5,019 人开始时间: 2016年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
5,019
主要终点
Number of patients with the incidence of parastomal bulging

研究概览

简要总结

The purpose of this study is to use routinely-collected health data from registers to examine the incidence of parastomal bulging (PB) at different time points in the first year after surgery for ileostomy or colostomy. Additionally, the purpose is to investigate risk factors for development of PB.

详细描述

Parastomal bulging (PB) in patients with ileostomy and colostomy in the Capital Region of Denmark up to one year after surgery is the primary outcome in this study. The investigators will use a register-based study design to evaluate routinely-collected health data from the Danish Stoma Database Capital Region (DSDCR). Incidence of PB one year post surgery and at different points of follow-up during the first year will be investigated using survival analysis. Potential risk factors will be investigated controlling for potential confounders. In order to include relevant variables on lifestyle, comorbidity, and physical status, data from the DSDCR will be linked to data from the Danish Anaesthesia Database.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Subject is registered in the Danish Stoma Database Capital Region
  • Is registered as having either ileostomy, jejunostomy, sigmoidostomy, or transversostomy

排除标准

  • Patients with urostomy or unknown stoma type

结局指标

主要结局

Number of patients with the incidence of parastomal bulging

时间窗: Up to 1 year after primary surgery

Parastomal bulging evaluated by stoma care nurses through symptoms, visual inspection, and stomal exploration. Parastomal bulging is evaluated at scheduled visits at stoma care clinics on postoperative days 30, 90, 180, and 365, and at any additional visits inbetween.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Rune Martens Andersen

PhD fellow

Rigshospitalet, Denmark

相似试验