Zinc Supplementation on Cellular Immunity in Thalassemia Major
Primary Purpose
Thalassemia, Splenectomy; Status, Immunosuppression
Status
Completed
Phase
Phase 4
Locations
Indonesia
Study Type
Interventional
Intervention
Zinc Sulfate
Sucrose Syrup
Sponsored by
About this trial
This is an interventional prevention trial for Thalassemia focused on measuring zinc supplementation, immunity, thalassemia
Eligibility Criteria
Inclusion Criteria:
- Thalassemia major patients
- Age > 12 years
- Agreed to participate and signed the informed consent
- No other comorbidity beside thalassemia
Exclusion Criteria:
- HIV positive patients
- Those in steroid medication
Sites / Locations
- Fakultas Kedokteran Universitas Indonesia
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Zinc sulfate
Sucrose syrup
Arm Description
Zinc sulfate is provided in the form of syrup at a dose of 1.5 mg/kg/day, maximum 50 mg/day.
Sucrose syrup is used as placebo, its provided in the form of syrup with similar appearance and taste.
Outcomes
Primary Outcome Measures
Patient's T-lymphocyte count
Measurement of patients CD4+ and CD8+ T-lymphocyte count in uL
Secondary Outcome Measures
Full Information
NCT ID
NCT03117192
First Posted
March 31, 2017
Last Updated
April 12, 2017
Sponsor
Fakultas Kedokteran Universitas Indonesia
1. Study Identification
Unique Protocol Identification Number
NCT03117192
Brief Title
Zinc Supplementation on Cellular Immunity in Thalassemia Major
Official Title
Zinc Supplementation on Cellular Immunity in Thalassemia Major
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
September 1, 2013 (Actual)
Primary Completion Date
February 1, 2014 (Actual)
Study Completion Date
February 1, 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fakultas Kedokteran Universitas Indonesia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Randomized controlled trial was conducted in post-splenectomy patients aged >12 years. Subjects are randomly assigned to two groups (zinc and placebo). 1.5 mg/kg/day (max 50 mg/day) of Zinc is administered.
Detailed Description
Thalassemia refers to a hereditary anaemic condition that occurs due to a single gene disorder resulting in a defect in globin production. Infection is an important cause of morbidity and mortality among thalassemia patients worldwide. Thalassemia patients are more prone to infection. Mechanism of this susceptibility is related to altered immune response compounded by splenectomy procedures common in patients with thalassemia. Zinc on the other hand plays important role in immune responses. This study aims to identify zinc supplementation to cellular immunity of splenectomized patients.
Randomized controlled trial was conducted in post-splenectomy patients aged >12 years. Subjects are randomly assigned to two groups (zinc and placebo). 1.5 mg/kg/day (max 50 mg/day) of Zinc is administered. Anamnesis, physical examination, and laboratory results such as peripheral blood, ferritin, transferrin saturation, serum zinc, immunologic markers for cellular immunity (lymphocyte count, CD4+ and CD8+ T lymphocyte count and functions) are evaluated at the start and end of the 12-week study.
Improvement in immune response is defined as an increase in the T lymphocyte count and CD4+ T lymphocyte count, decrease in CD8+, and increase in the CD4+/CD8+ ratio.12 The mean reference value for CD4+/CD8+ ratio is 1.4 (SD 0.6).15 CD4+ T lymphocyte function refers to its ability to synthesize IL-2 and TNF-α following exposure to 100 µL phytohaemagglutinin with proportions measured using flow cytometry. Meanwhile, CD8+ T lymphocyte function refers to its ability to synthesize IL-2 and TNF-α following exposure to 100 µL phytohaemagglutinin measured using flow cytometry.
The frequency of blood transfusion is calculated from the medical records of the subjects during the past 1 year, which is grouped as follows:
Seldom receive blood transfusions, if within a time period of one year the subject received blood transfusions of < 1 time.
Sometimes receive blood transfusions, if within a time period of one year the subject received blood transfusions of 2 - 3 times.
Often receive blood transfusions, if within a time period of one year the subject received blood transfusions of > 4 times.
Analysis was conducted using Statistical Package for Social Sciences (SPSS) version 20.0. Changes in immunologic parameters between the two groups that are numeric will be analysed using paired t-test for variables with a normal distribution, and Mann-Whitney test for numeric variables with non-normal distributions.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thalassemia, Splenectomy; Status, Immunosuppression
Keywords
zinc supplementation, immunity, thalassemia
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
This interventional study is a randomized controlled trial comparing the parallel provision of zinc and placebo in 2 groups of splenectomized thalassemia major patients.
Masking
ParticipantCare ProviderInvestigator
Masking Description
Secretary to the department held an envelope that shows sample allocation after randomization. The envelope is only revealed after data gathering is finished.
Allocation
Randomized
Enrollment
58 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Zinc sulfate
Arm Type
Experimental
Arm Description
Zinc sulfate is provided in the form of syrup at a dose of 1.5 mg/kg/day, maximum 50 mg/day.
Arm Title
Sucrose syrup
Arm Type
Placebo Comparator
Arm Description
Sucrose syrup is used as placebo, its provided in the form of syrup with similar appearance and taste.
Intervention Type
Drug
Intervention Name(s)
Zinc Sulfate
Intervention Description
Zinc supplementation in syrup form
Intervention Type
Drug
Intervention Name(s)
Sucrose Syrup
Intervention Description
Sucrose as placebo, with same taste and consistency as zinc
Primary Outcome Measure Information:
Title
Patient's T-lymphocyte count
Description
Measurement of patients CD4+ and CD8+ T-lymphocyte count in uL
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Thalassemia major patients
Age > 12 years
Agreed to participate and signed the informed consent
No other comorbidity beside thalassemia
Exclusion Criteria:
HIV positive patients
Those in steroid medication
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Teny T Sari, M.D., PhD
Organizational Affiliation
Faculty of Medicine University of Indonesia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fakultas Kedokteran Universitas Indonesia
City
Jakarta Pusat
State/Province
Jakarta
ZIP/Postal Code
10430
Country
Indonesia
12. IPD Sharing Statement
Plan to Share IPD
No
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Zinc Supplementation on Cellular Immunity in Thalassemia Major
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