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临床试验/NCT03865264
NCT03865264终止不适用

Living Organ Donor Recovery Enhancement Program

Baylor Research Institute1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2017年4月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
21
试验地点
1
主要终点
Level of pain experienced daily

研究概览

简要总结

The purpose of the study is to test if using these living donor-specific pre-transplant resources would lead to a better and faster recovery post-transplant.

详细描述

Donor safety and outcomes are the chief concerns of programs performing living donor liver and kidney transplantation. The protection of donors from physical and emotional harm has been a fundamental principle in living donor liver and kidney donation from the beginning. The safety of living donor hepatectomy and nephrectomy has been established. The risks associated with the donation have been deemed acceptable by the transplant community.

The investigators would like to move beyond the safety of the operation and address the most important post-operative issues that potentially cause donors physical and emotional stress: these include pain control, appropriate nutrition for optimal liver regeneration and physical/functional recovery, fatigue, time to return to normal physical and work activity, and difficulties coping with recovery and any possible complications. The goal of conducting this study is to create a program of pre- and post-operative interventions to enhance recovery so that patients can return to their normal quality of life as soon as possible. Currently there is no literature on programs to enhance living donor care and recovery.

This study will be conducted to determine if interventions during the pre-operative (a minimum of four weeks in an exercise program), intra-operative (anesthesia), and post-operative (pain management) stages have an effect on liver and kidney donor patients' quality of life and return to baseline functional status.

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

  • Ages ≥ 18 years
  • Cleared by a physician to participate in an exercise program
  • Approved for evaluation to be a living liver or kidney donor
  • Subjects willing and able to comply with the protocol procedures for the duration of the study, including the exercise regimen and scheduled follow-up visits
  • Subjects who have given IRB-approved written informed consent, prior to any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to future medical care

排除标准

  • Any co-morbidity restricting the subject's ability to walk alone
  • Pregnant or breast-feeding women

研究组 & 干预措施

Living Liver donor

Active Comparator

Recovery enhancement program:

  1. At least 6 weeks of physical and relaxation skills training pre-transplant.
  2. Taking nutritional drink for 5 days before and after the surgery.
  3. Opioid sparing pain management.

干预措施: Recovery Enhancement Program (Other)

Living Kidney donor

Active Comparator

Recovery Enhancement Program

  1. At least 4 weeks of physical and relaxation skills training pre-transplant.
  2. Taking nutritional drink for 5 days before and after the surgery.
  3. Opioid sparing pain management.

干预措施: Recovery Enhancement Program (Other)

Living Kidney donor (Control)

No Intervention
  1. Subjects maintain the same lifestyle without practicing physical training, relaxation skills or nutritional drink before and after the surgery.
  2. To control post-op pain, subject will use medication per standard of care, including PCA pump.

结局指标

主要结局

Level of pain experienced daily

时间窗: From day of admission into ICU (post-hepatectomy) up to day of hospital discharge (4-14 days post-hepatectomy)

level of pain per numerical rating pain scale (scale 0-10) with 0 being no pain and 10 being severe pain.

Incidence of Post-operative hospital re-admissions

时间窗: From post-transplant discharge to 1 year follow-up

Number of post-operative hospital re-admissions

RAND SF-36 questionnaires

时间窗: From month 1 to month 12 post transplantation.

Post-operative emotional stress

Opioid usage

时间窗: From day of hospital discharge (post-hepatectomy) up to 1 year post hepatectomy.

Number of participants that require using opioid medication to treat abdominal and incisional pain post hepatectomy, medication strength and frequency of use.

Duration to return of daily activities

时间窗: From day of hospital discharge to 1 year follow up.

Duration to return of daily activities

Duration in ICU

时间窗: From day admission into ICU up to day of discharge to hospital floor or 14 days post hepatectomy, whichever came first.

Duration in ICU post-hepatectomy

RAND SF-36 questionnaires

时间窗: From day of enrollment in the study (at least 4 weeks before surgery) up to 1 day prior to hepatectomy.

Pre-operative emotional stress

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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