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Clinical Trials in Italy / NCT06905704
Recruiting Observational

Impact of Stem Cell Donation on Unrelated and Related Donors' Health.

NCT06905704 · tracked via the Priya Life Science Italy tracker
Sponsor
Fondazione IRCCS Policlinico San Matteo di Pavia
Phase
Observational
Started
2023-02-03
Last updated
2025-04-01

Condition(s) studied

Stem Cell Donors

Study summary

Haematopoietic stem cell donation represents a unique chance for curing patients affected with onchohaematologic and inherited diseases.If a related donor is unavailable a unrelated donor must be used. For both categories an accurate physical and laboratory examination is mandatory to establish the eligibility to bone marrow or peripheral blood stem cell collection since side effects related to donation may occur. To ensure high standards of safety and satisfaction of unrelated stem cells donors dedicated guidelines are available. On the other hand, there is no unambiguous guidance on the management of the related donor and published data on donation and long term follow-up are scarce.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Family donors ≥18 years referred by the Hematology and Oncohematology Transplant Center Pediatric of the Foundation of Centro Donatori -SIMT, following the national and international guidelines after medical evaluation * Volunteer donors from IBMDR registry ≥18 years, following the national and international guidelines after medical evaluation Exclusion Criteria: * Donors 18 \< years

Primary outcome measure(s)

  • safety of stem cell donation — From enrollment to 30 days after stem cell donation
    The proportion of overall serious adverse reactions/events (number of patient-reactions out of the total number of patients)

Trial sites (1)

FacilityCityRegionStatus
Fondazione IRCCS Policlinico San Matteo di Pavia Pavia Pavia Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06905704 on ClinicalTrials.gov ↗ ← All trials in Italy