Completed

Live Donor Renal Donation for Allotransplantation

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Who is being recruted

Over 18 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: May 1999
See protocol details

Summary

Principal SponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Last updated: December 9, 2019
Sourced from a government-validated database.Claim as a partner

Study start date: May 17, 1999

Actual date on which the first participant was enrolled.

This protocol is designed to facilitate the enrollment of healthy individuals to serve as renal allograft donors for subjects undergoing protocol renal transplantation at the NIH. Donation will be allowed for altruistic purposes only.

NCT00001856
Principal SponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Last updated: December 9, 2019
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

260 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

INCLUSION CRITERIA: Willingness to donate without evidence of secondary gain, coercion, or conflict of interest. Age greater than or equal to 18 years ABO compatible with recipient Normal renal function with a 24hr creatinine clearance greater than 80ml/min/1.73m(2). Willingness and legal ability to give informed consent Recipient is enrolled in a NIH protocol for transplantation or has been established as a candidate for receipt of an altruistic or paired donation through the Washington Regional Organ Procurement Agency donor program. EXCLUSION CRITERIA: Hypertension Pregnancy History of stroke Active tuberculosis History of active malignancies except basal cell carcinoma of the skin. Major anticipated illness or organ failure incompatible with survival after nephrectomy Functionally significant coronary artery disease. Active kidney stones Proteinuria (greater than 250mg/24hr)

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, United StatesOpen National Institutes of Health Clinical Center, 9000 Rockville Pike in Google Maps
CompletedOne Study Center