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Trial record 1 of 1 for:    A Multicenter Study of Hematopoietic Stem Cell Donor Safety and Quality of Life
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Stem Cell Related Donor Safety Study (RDSafe)

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ClinicalTrials.gov Identifier: NCT00948636
Recruitment Status : Completed
First Posted : July 29, 2009
Last Update Posted : June 14, 2017
Sponsor:
Collaborators:
Information provided by (Responsible Party):

Study Description
Brief Summary:

The study tests the hypothesis that related hematopoietic stem cell donors are at a higher risk for acute medical and psychological toxicity associated with the donation process compared to adult unrelated hematopoietic stem cell donors.

The study will also assess the hypothesis that young (<18 years) and older (>60 years) related donors are at increased risk for toxicity associated with donation compared to younger adult donors by describing the adverse events reported in these populations.

An ancillary study of the psychological impact of donation on health-related quality of life (HRQoL) will enroll related donors and compare them to an age-matched normative cohort.


Condition or disease
Related Hematopoietic Stem Cell Donors

Study Design

Study Type : Observational
Actual Enrollment : 1812 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: A Multicenter Study of Hematopoietic Stem Cell Donor Safety and Quality of Life
Study Start Date : January 2010
Primary Completion Date : August 2015
Study Completion Date : September 2016
Groups and Cohorts

Group/Cohort
Related Donors
Related Hematopoietic Stem Cell Donors


Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
participating institutions (transplant centers)
Criteria

Inclusion Criteria:

  • Donors of any age providing either a first or second BM or PBSC donation
  • Meet donation criteria per institution policies and procedures
  • Willing to receive phone follow-up at 1, 6, and 12 months
  • Signed informed consent for study participation

For the HRQoL ancillary study, inclusion criteria:

  • Related donors age greater than or equal to 5, eligible and consented to the primary trial by the above listed inclusion criteria
  • Donors competent to answer psychological assessment questions by themselves, or if a child, should be able to respond to psychological assessment questions and have an appropriate proxy also able to complete the HRQoL proxy interview
  • English speaking
  • Access to a telephone
  • Willing to participate in pre-donation, 1 month and 1 year follow-up interviews
  • Signed informed consent for study participation in ancillary study

Exclusion Criteria:

  • Per institutional guidelines
  • Donors providing unstimulated peripheral blood stem cells or lymphocytes

For the HRQoL ancillary study, exclusion criteria:

  • Children less than or equal to 4 years of age
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00948636


  Show 52 Study Locations
Sponsors and Collaborators
Center for International Blood and Marrow Transplant Research
National Institutes of Health (NIH)
University of Utah
University of Pittsburgh
Investigators
Principal Investigator: Michael A Pulsipher, M.D. Children's Hospital Los Angeles
More Information

Responsible Party: Center for International Blood and Marrow Transplant Research
ClinicalTrials.gov Identifier: NCT00948636     History of Changes
Other Study ID Numbers: 06-DON
First Posted: July 29, 2009    Key Record Dates
Last Update Posted: June 14, 2017
Last Verified: July 2016