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Search / Trial NCT04917978

Association of Hb F Level With Clinical Severity of Beta Thalassemia

Launched by NANFANG HOSPITAL, SOUTHERN MEDICAL UNIVERSITY · Jun 7, 2021

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying how the levels of a specific type of hemoglobin, called Hb F, relate to the severity of beta thalassemia, a blood disorder that affects how your body produces hemoglobin. The researchers want to understand if higher levels of Hb F can help lessen the effects of this condition in patients. Beta thalassemia can vary in how it affects people, and this study aims to see if there’s a connection between Hb F levels and how severe the disease is in different patients.

To participate in this trial, individuals must be diagnosed with beta thalassemia. Unfortunately, those with iron deficiency anemia cannot join. If eligible, participants will likely undergo tests to measure their Hb F levels and may provide information about their health. The study is currently looking for individuals of all ages and genders to help advance our understanding of beta thalassemia and potentially improve treatment options in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Diagnosed with beta-thalassemia
  • Exclusion Criteria:
  • Iron Deficiency Anemia

About Nanfang Hospital, Southern Medical University

Nanfang Hospital, affiliated with Southern Medical University, is a leading medical institution in China renowned for its comprehensive clinical services and commitment to advancing healthcare through research and education. As a clinical trial sponsor, Nanfang Hospital leverages its state-of-the-art facilities and a multidisciplinary team of expert researchers to conduct innovative studies aimed at improving patient outcomes and contributing to the global medical community. The hospital's focus on ethical standards and patient safety ensures that all trials are conducted with the highest level of integrity and scientific rigor.

Locations

Guangzhou, Guangdong, China

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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