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临床试验/NCT07231666
NCT07231666已完成不适用

Goldilocks' Zone: Optimised Osmolality in Supplements for the Patient With an Ileostomy

University of Aarhus4 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2021年11月11日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
4
主要终点
ileostomy output

研究概览

简要总结

Quasi-randomized, crossover intervention study, testing osmolality in oral drinks and effect on 6-hours ileostomy output in adult patients with an ileostomy

详细描述

14 patients with ileostomies were included in a quasi-randomized, crossover intervention study. Each patient ingested between 3-18 different supplements during separate 6-hours intervention periods. Ileostomy output and urine volume will be collected. Outcome measures include faecal wet-weight, urine volume, electrolytes, osmolality, and body composition measured with bioelectrical impedance analysis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Supportive Care
盲法
Single (Participant)

盲法说明

The patients were randomised to receive either the hypo-osmolar or hyper-osmolar in their first intervention. Microsoft Excel feature "RAND" (Microsoft version 16) was used to randomize oral supplements. Each supplement was assigned a number. Every time a patient agreed to one or two more intervention periods, two supplements were randomized. One of the primary investigators (JQ) enrolled and randomized supplements to the patients

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

  • age 18 years or higher
  • ileostomy formed at least 8 weeks before enrolment
  • consent to participate

排除标准

  • known chronic kidney disease
  • known diabetes mellitus
  • too long driving distance
  • parenteral nutrition/fluid more than 6 litres per month

结局指标

主要结局

ileostomy output

时间窗: 6 hours

ileostomy output (wet weight feces grams)

次要结局

  • natriuresis(6 hours)
  • urine sodium(6 hours)
  • urine osmolality(6 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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