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临床试验/NCT06058442
NCT06058442招募中3 期

The Pancreatic Enzymes After Gastrectomy Trial

University of Leipzig18 个研究点 分布在 1 个国家目标入组 188 人开始时间: 2024年1月24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
招募中
发起方
入组人数
188
试验地点
18
主要终点
Disease specific quality of life (QOL)

研究概览

简要总结

This trial evaluates the effects (e.g. on quality of life, weight) of NORTASE® compared to standard care of patients who have undergone gastrectomy.

研究设计

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

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

  • Gastrectomy (total and partial distal); at least > 50 % of the stomach must be resected
  • Age 18 or older
  • Written informed consent

排除标准

  • Indication for pancreas enzyme therapy
  • Gastrectomy with palliative intention
  • UICC (Union for International Cancer Control) Stage IV gastric malignancy
  • Malnutrition of other aetiology
  • Life expectancy < 12 months
  • Known lactose intolerance
  • Known hereditary galactose intolerance
  • Patients on alpha-glucosidase inhibitors (AGIs)
  • Acute pancreatitis
  • Acute episode of chronic pancreatitis
  • Known hypersensitivity to moulds (mould allergy) or any other ingredient of NORTASE®
  • Participation in competing interventional trials may be allowed under circumstances
  • Patients under legal supervision or guardianship
  • Patients who are dependent on the investigator or the medical staff of the trial team or the coordinating investigator or the sponsor
  • Fertile women (within two years of their last menstruation) without appropriate contraceptive measures (implanon, injections, oral contraceptives, intrauterine devices, partner with vasectomy) while participating in the trial
  • Pregnant or nursing women
  • Suspected lack of compliance
  • Patients who were already enrolled in the trial

研究组 & 干预措施

NORTASE®

Experimental

干预措施: NORTASE® (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Disease specific quality of life (QOL)

时间窗: 6 months

This is the physical sub-score from the European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (EORTC-QLQ-C30) and ranges from 0 (lowest physical functioning) to 100 (highest physical functioning).

次要结局

  • Vitamin K(6 months)
  • HbA1c(6 months)
  • Vitamin B12(6 months)
  • Serum haemoglobin(6 months)
  • Albumin(6 months)
  • Glucose(6 months)
  • Cholesterol(6 months)
  • Nutritional supplementation or weight loss(6 months)
  • Weight(6 months)
  • Vitamin A(6 months)
  • Vitamin D(6 months)
  • Vitamin E(6 months)
  • Total protein(6 months)

研究者

发起方
University of Leipzig
申办方类型
Other
责任方
Principal Investigator
主要研究者

Albrecht Hoffmeister

Prof. Dr. med.

University of Leipzig

研究点 (18)

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