跳至主要内容
临床试验/NCT04932148
NCT04932148招募中不适用

The INCremental Dialysis to Improve Health Outcomes in People Starting Haemodialysis (INCH-HD) Study: a Randomised Controlled Trial

The University of Queensland32 个研究点 分布在 2 个国家目标入组 372 人开始时间: 2022年7月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
372
试验地点
32
主要终点
Heath related quality of life

研究概览

简要总结

The INCH-HD trial will test if incremental HD preserves the quality of life of patients and families and is a safe, practical, cost effective treatment option.

详细描述

Kidney failure is a growing public health problem and fatal unless treated with dialysis or transplantation. Haemodialysis is the most common treatment for kidney failure in Australia and globally. Patients find haemodialysis extremely burdensome due to symptoms like fatigue, pain, cramps and poor quality of life that generally equates to <60% of full health. Furthermore, haemodialysis is associated with an extremely high mortality (<50% survive 5 years), particularly in the first 3-6 months of starting haemodialysis, which is likely linked to the rapid loss of patients' own kidney function when starting haemodialysis abruptly at three sessions/week. Observational studies suggest that starting haemodialysis incrementally at two sessions/ week is associated with lower mortality and better preservation of patients' remaining kidney function while offering many patient-important advantages, including dialysis free time and ability to work. However, robust evidence to recommend this incremental approach is lacking.

The INCH-HD study is an investigator-initiated, international, multicentre, prospective, adaptive, randomised, open-label, parallel group, non-inferiority trial. The primary objective of the study is to demonstrate whether incremental HD is non-inferior to conventional HD for the patient-important outcome of quality of life measured using Kidney-specific component of the Kidney Disease Quality of Life - Short Form measurement (KDQOL-SF) at 6 months from dialysis commencement.

The study will recruit a total of 372 participants across HD centres in Australia, and Canada. The outcomes of this trial will will provide urgently needed high quality evidence on whether starting haemodialysis incrementally at two sessions/week compared to the conventional three sessions/week can safely reduce the physical, financial and quality-of life burden on patients, lower early mortality rates and slow loss of kidney function while increasing haemodialysis capacity and reducing costs.

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
Single (Outcomes Assessor)

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

  • Adults (≥ 18 years of age) and
  • Commencing HD as their initial dialysis therapy and
  • Able to give informed consent

排除标准

  • Urine output <0.5Litres/day
  • Unlikely to be on HD for ≥1 year.

研究组 & 干预措施

Incremental HD

Experimental

Participants randomised to incremental HD will commence HD twice weekly and continue until an indication for an increase to three sessions/week (trigger point) is reached.

干预措施: Incremental HD (Other)

Conventional HD

Other

Participants randomised to conventional HD will commence HD thrice weekly from the first HD session.

干预措施: Conventional HD (Other)

结局指标

主要结局

Heath related quality of life

时间窗: 6 months

This will be measured using Kidney-specific component (KSC) of the Kidney Disease Quality of Life Short Form (KDQOL-SF) V1.3 questionnaire. The KSC is the mean of the 11 domains of the kidney-disease specific items of KDQOL-SF. Scores are transformed onto a 0-100 range, where a higher score reflects a better quality of life.

次要结局

  • Total hospital days(Baseline to 18 months)
  • Time to death(Baseline to 18 months)
  • Healthcare resource utilisation(Baseline to 18 months)
  • Time to major cardiovascular event (MACE)(Baseline to 18 months)
  • Number of non-elective hospital admissions(Baseline to 18 months)
  • Symptom scores(Baseline, 3, 6, 9, 12, 15 and 18 months)
  • Fatigue(Baseline, 3, 6, 9, 12, 15 and 18 months)
  • Vascular access(Baseline to 18 months)
  • Residual kidney function (RKF)(Baseline, 3, 6, 12 and 18 months)
  • Incidence of all-cause mortality(Baseline to 18 months)
  • Nutritional Status(Baseline, 6, 12 and 18 months)
  • Healthcare costs(Baseline to 18 months)
  • Heath related quality of life using Kidney Disease Quality of Life Short Form (KSQOL-SF) questionnaire(Baseline, 3, 6, 9, 12, 15 and 18 months)
  • Heath related quality of life using EuroQol 5-dimension 5-level (EQ-5D-5L) questionnaire(Baseline, monthly to 18 months)
  • Number of hospital admissions(Baseline to 18 months)
  • Adverse events and side-effects(Baseline to 18 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (32)

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