International Registry of Patients With Alpha Thalassemia

NCT04872179 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2025-04-04

No results posted yet for this study

Summary

This is an international prospective registry of patients with Alpha thalassemia to understand the natural history of the disease and the outcomes of fetal therapies, with the overall goal of improving the prenatal management of patients with Alpha thalassemia.

Conditions

  • Alpha-Thalassemia
  • Alpha Thalassemia Major
  • Alpha Thalassemia Minor

Sponsors & Collaborators

Principal Investigators

  • Tippi C MacKenzie, MD · University of California, San Francisco

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2027-01-31
Completion
2037-01-31

Countries

  • United States

Study Locations

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Entities

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 NCT04872179 on ClinicalTrials.gov