Prevalence of Hemoglobinopathies Associated With Significant Hb Variants in the Chattogram Region of Bangladesh

NCT ID: NCT07207551

Last Updated: 2025-10-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

760 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-06-01

Study Completion Date

2025-09-04

Brief Summary

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Hemoglobinopathies represent a collection of genetic conditions that influence the structure or synthesis of haemoglobin, the protein found in red blood cells that facilitates oxygen transport from the lungs throughout the body. This research proposal presents a study evaluating the prevalence of hemoglobinopathies and their significant haemoglobin variants within a specific population. The research will employ a cross-sectional study design, recruiting participants through community outreach efforts and healthcare facilities while obtaining informed consent. Data will be collected with the utmost precision and rigor, using advanced screening techniques such as high-performance liquid chromatography (HPLC), capillary electrophoresis, and molecular analysis. The gathered data will be processed to assess haematological parameters, including RBC, Iron Ferritin, TIBC, electrophoresis profiles (HbA, HbA2, HbE, HbF), MCV, MCHC, and PCV among individuals with hemoglobinopathies (HbE disease/trait, Beta thalassemia disease/trait, heterozygous HPFH, HbE-beta thal). They will examine variations relative to demographic factors. The expected results will have substantial clinical and public health consequences by enhancing genetic counselling, informing clinical decision-making, and strengthening public health initiatives.

Detailed Description

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Hemoglobinopathies are genetic disorders affecting the structure or production of hemoglobin, the oxygen-carrying protein in red blood cells. This study aims to determine the prevalence and major variants of hemoglobinopathies in a target population using a cross-sectional design. Participants will be recruited through community outreach and healthcare facilities with informed consent. Screening will involve advanced techniques such as HPLC, capillary electrophoresis, and molecular analysis, alongside hematological assessments (RBC, ferritin, TIBC, MCV, MCHC, PCV, and hemoglobin profiles: HbA, HbA2, HbE, HbF). Findings will be analyzed in relation to demographic factors.

Conditions

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Hemoglobinopathies

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Residents of the Chattogram metropolitan area.
* All ages and both sexes with informed consent.
* Willing to provide venous blood samples.
* No blood transfusion in the past 3 months.

Exclusion Criteria

* Refusal or withdrawal of consent.
* Blood transfusion within the last 3 months.
* Pregnant women.
* Inadequate or hemolyzed blood samples.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bangladesh Bioscience Research Group

NETWORK

Sponsor Role lead

Responsible Party

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Pair Ahmed Jiko

Lab-Incharge (Biochemist)

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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PAIR AHMED JIKO, Lab-Incharge (Biochemist)

Role: PRINCIPAL_INVESTIGATOR

Institute Of Applied Health Sciences Hospital-USTC (Ex-BBMH)

Locations

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University of Science and Technology Chittagong (USTC)

Khulshi, Chattogram, Bangladesh

Site Status

Countries

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Bangladesh

Other Identifiers

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BBMH/January/2024/024

Identifier Type: OTHER

Identifier Source: secondary_id

BBMH/2024/RP-2412

Identifier Type: -

Identifier Source: org_study_id

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