Genetic Variants Affecting the Clinical Severity of Beta Thalassemia
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ClinicalTrials.gov Identifier: NCT04918056 |
Recruitment Status : Unknown
Verified May 2021 by Nanfang Hospital, Southern Medical University.
Recruitment status was: Recruiting
First Posted : June 8, 2021
Last Update Posted : June 11, 2021
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Condition or disease | Intervention/treatment |
---|---|
Beta Thalassemia | Diagnostic Test: Hematological Analysis and Genetical Analysis |
Study Type : | Observational |
Estimated Enrollment : | 1300 participants |
Observational Model: | Cohort |
Time Perspective: | Retrospective |
Official Title: | Screening and Identification of Genetic Modifiers Which Affecting the Phenotype Severity of Beta Thalassemia Patients |
Actual Study Start Date : | January 1, 2017 |
Estimated Primary Completion Date : | January 11, 2022 |
Estimated Study Completion Date : | June 25, 2023 |
Group/Cohort | Intervention/treatment |
---|---|
beta thalassemia patients |
Diagnostic Test: Hematological Analysis and Genetical Analysis
Hematological Analysis: Hematological parameters were determined with an automated hematology analyzer (Sysmex, Japan), and hemoglobin analysis was performed with either high-performance liquid chromatography (Bio-Rad, USA) or capillary electrophoresis (Sebia, France and Helena, USA). Genetical Analysis: Genomic DNA was extracted from peripheral blood (PB) by using a standard phenol/chloroform method. The genotypes of samples are analyzed by NGS assay. |
- Genetic variants which could influence the phenotype of beta thalassemia [ Time Frame: 1 year ]Identified a group of single-nucleotide polymorphisms (SNPs) that contribute to β-thalassemia
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Ages Eligible for Study: | Child, Adult, Older Adult |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Inclusion Criteria:
- Diagnosed with β-thalassemia
Exclusion Criteria:
- Iron Deficiency Anemia
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): NCT04918056
Contact: Xiangmin Xu, Prof. Dr. | (20) 61648293 ext 86 | xixm@smu.edu.cn |
China, Guangdong | |
Southern Medical University | Recruiting |
Guangzhou, Guangdong, China, 510515 | |
Contact: Xiangmin Xu, Prof. Dr. (20) 61648293 ext 86 xixm@smu.edu.cn |
Responsible Party: | Nanfang Hospital, Southern Medical University |
ClinicalTrials.gov Identifier: | NCT04918056 |
Other Study ID Numbers: |
PDD-Beta thalassemia |
First Posted: | June 8, 2021 Key Record Dates |
Last Update Posted: | June 11, 2021 |
Last Verified: | May 2021 |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
beta thalassemia Hb F Onset age Genetic Modifier |
Thalassemia beta-Thalassemia Anemia, Hemolytic, Congenital Anemia, Hemolytic |
Anemia Hematologic Diseases Hemoglobinopathies Genetic Diseases, Inborn |