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临床试验/NCT03348709
NCT03348709已完成不适用

Does Osmolality of Oral Supplements Affect Stoma Output and Natriuresis in Patients With an Ileostomy?

University of Aarhus2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2017年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
8
试验地点
2
主要终点
Stoma output

研究概览

简要总结

This double-blinded, active comparator, cross-over intervention study tested the impact of two different oral supplements on ileostomy output volume and urinary sodium excretion and intestinal aquaporin expression in eight compensated patients with an ileostomy and not on home parenteral Nutrition or fluid support.

详细描述

Patients with an ileostomy may experience fluid and electrolyte imbalances sedondary to an unregulated intestinal loss of water and electrolytes. The osmolality of oral supplements may affect these losses. In a double-blinded, active comparator, cross-over intervention study, the investigators test the effects of substituting 800 ml of the usual fluid intake with an intake of either an isoosmolar (300 mOsm/kg) or hyperosmolar (700 mOsm/kg) supplement during 48 hours, following baseline data collection before both intervention periods. Outcome measures were stoma output volume, 24-hour urine and urinary sodium excretion, and intestinal aquaporin 3 and 8 expressions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Randomisation by Third party; Unblinded study nurse to mix and deliver study product; masking of product to ensure comparable palatability and appearance; blinding to analyses

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 more
  • ilestomy established 6 weeks or more prior to inclusion
  • able to drink at least 100 ml fluid per 24 hours
  • i known inflammatory bowel disease, clinical remission judged by physician's global assessment (PGA)
  • less than 5 kg self-reported weight change during the past 3 months

排除标准

  • self-reported intolerance to dairy products, including lactose
  • known renal insufficiency, defined by an eGFR less than 30 ml/min
  • known diabetes mellitus, defined by an HbA1C > 48 mmol/mol (6.5%)
  • current enteral tube feeding or parenteral fluid or Nutrition support more than twice weekly

研究组 & 干预措施

Isoosmolar

Experimental

Iso-osmolar oral supplement (276 mOsm/kg)

干预措施: Isoosmolar (Dietary Supplement)

Hyperosmolar

Active Comparator

Hyper-osmolar oral supplement (681 mOsm/kg)

干预措施: Hyperosmolar (Dietary Supplement)

结局指标

主要结局

Stoma output

时间窗: 24 hours

24 hour stoma output weight

次要结局

  • 24-hour urinary sodium excretion(24 hours)
  • 24-hour urine production(24 hours)

研究者

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

Christian Hvas

MD PhD, associate professor

University of Aarhus

研究点 (2)

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