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Living Organ Donor Recovery Enhancement Program

NCT03865264 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2026-01-27

No results posted yet for this study

Summary

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.

Conditions

  • Living Liver and Kidney Donors

Interventions

OTHER

Recovery Enhancement Program

Behavioral, nutritional, physical and opioid-reduction pain medication

Sponsors & Collaborators

  • Baylor Research Institute

    lead OTHER

Principal Investigators

  • Guiliano Testa, MD · Simmons Transplant Institute, Baylor University Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-04-20
Primary Completion
2024-01-22
Completion
2024-01-22

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03865264 on ClinicalTrials.gov