Evaluation of Healthy Volunteer Marrow Donors Participating in the National Marrow Donor Program (NMDP)

Sponsor
National Institutes of Health Clinical Center (CC) (NIH)
Overall Status
Completed
CT.gov ID
NCT00001451
Collaborator
(none)
57
1
190.7
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Study Details

Study Description

Brief Summary

Individuals interested in becoming prospective bone marrow donors and joining the Registry of the National Marrow Donor Program (NMDP) should do so by calling 301-496-0572, the phone number of the NIH Marrow Donor Center. An appointment will be made to have a health history taken and to have a buccal swab collected for tissue (HLA) typing. The current protocol only involves donors already registered with the NMDP, who have been identified as "perfect matches" for an unrelated patient requiring a bone marrow transplant, and who require expedited medical evaluation prior to marrow collection.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The National Marrow Donor Program (NMDP) was established in 1987 in order to (1) create a registry of volunteer, prospectively tissue-typed, unrelated bone marrow donors, (2) facilitate the performance of matched unrelated donor marrow transplants through a coordinated circuit of Donor Centers, Collection Centers and Transplant Centers throughout the United States, and (3) evaluate the outcome of such transplants and identify future areas of research in the field of unrelated donor marrow transplants. The NIH Marrow Donor Center, a participant in the NMDP, is currently the second largest hospital-based Donor Center in the nation, with approximately 55,900 active donors on its registry. 402 NIH unrelated donors to date have undergone 429 marrow or blood stem cell harvest for an NMDP recipient, and the current rate of such harvests is three per month. Once an HLA-matched donor in the NIH Donor Center registry is identified through the NMDP computer network, the donor must undergo a medical evaluation to determine suitability for marrow harvest. This evaluation consists of a medical history, a physical examination, routine blood work, EKG, chest x-ray, and urinalysis, and generally takes 4 to 6 weeks. A "third party" non-NIH physician usually performs the evaluation, with the costs reimbursed by the NMDP. Occasionally, an expedited evaluation of an unrelated donor must be performed, due to the urgency of the need for a transplant in the recipient, and there is insufficient time to accomplish this work-up using the routine "third-party" physician's office mechanism. This protocol shall provide a means by which prospective NIH unrelated marrow donors participating in the NMDP program can undergo an expedited medical evaluation to determine suitability for marrow donation. It is expected that not more than 5 to 10 donors per year shall require such expedited evaluation.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    57 participants
    Official Title:
    Evaluation of Healthy Volunteer Marrow Donors Participating in the National Marrow Donor Program (NMDP)
    Study Start Date :
    Mar 14, 1995
    Study Completion Date :
    Feb 1, 2011

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      18 Years to 60 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      • INCLUSION CRITERIA:

      Age 18-60.

      Must meet same criteria as that of a volunteer blood donor.

      EXCLUSION CRITERIA:

      History of hepatitis.

      History of intravenous use of illicit drugs.

      History of activities that increase the risk of exposure to HIV or hepatitis viruses.

      Confirmed positive test for HIV

      Inability to tolerate general anesthesia.

      Obesity.

      Hypertension.

      Asthma.

      Diabetic patients will be excluded.

      Pregnant patients will be excluded.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda Maryland United States 20892

      Sponsors and Collaborators

      • National Institutes of Health Clinical Center (CC)

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00001451
      Other Study ID Numbers:
      • 950123
      • 95-CC-0123
      First Posted:
      Nov 4, 1999
      Last Update Posted:
      Jul 2, 2017
      Last Verified:
      Feb 1, 2011

      Study Results

      No Results Posted as of Jul 2, 2017