跳至主要内容
临床试验/NCT05760339
NCT05760339招募中不适用

Preoperative Intermittent Fasting Versus Carbohydrate Loading to Reduce Insulin Resistance: a Randomised Controlled Trial

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)2 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2023年3月20日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
75
试验地点
2
主要终点
Insulin resistance on postoperative day 1

研究概览

简要总结

The purpose of this study is to investigate whether time-restricted feeding, a form of intermittent fasting, before surgery improves insulin resistance around the time of surgery, compared to carbohydrate drinks and standard fasting before surgery.

详细描述

Patients in the Time-Restricted Feeding (TRF) group will follow a daily TRF regimen consisting of an 8h ad libitum eating period and a 16h water fasting period during the last two weeks before surgery, followed by routine preoperative fasting before surgery.

Patients in the CarboHydrate Loading (CHL) group will follow their usual diet in the pre-surgical weeks and will receive a maltodextrin beverage on the evening before surgery, as well as two hours before induction of anaesthesia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

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

  • Undergoing elective orthopaedic surgery;
  • Intermediate, major or complex surgery according to the Surgical Outcome Risk Tool (SORT; http://www.sortsurgery.com/) severity of surgery classification;
  • Scheduled for surgery at least 17 days from the date of screening;
  • Motivated to follow a time restricted feeding regimen.
  • Willing and able to provide written informed consent.

排除标准

  • History of diabetes mellitus;
  • History of feeding or eating disorders;
  • History of delayed gastric emptying or gastro-oesophageal reflux
  • Active malignancy
  • Patients classified as ASA IV by the attending anaesthetist;
  • BMI < 18.5 or ≥ 35;
  • Outpatient or day case surgery;
  • Palliative surgery;
  • Participation in another clinical trial that is interfering with the procedures or outcomes of the PRINCESS trial;
  • Patients unable to fully comply to study needs (e.g. legally incapable patients or patients unable to communicate in Dutch).

结局指标

主要结局

Insulin resistance on postoperative day 1

时间窗: Postoperative day 1

Insulin resistance according to the updated homeostasis model assessment of insulin resistance (HOMA2-IR)

次要结局

  • Difference in HOMA2-IR(From baseline to day of surgery, from baseline to postoperative day 1 and from day of surgery to postoperative day 1.)
  • Beta-cell function(The day of surgery and the first postoperative day)
  • Patient wellbeing(During the two weeks preoperatively, until one day postoperatively)

研究者

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

B Preckel

Prof. dr.

Amsterdam UMC, location AMC

研究点 (2)

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