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Effect of Zinc Supplementation on Hyperhomocysteinemia Compared to Folic Acid in CKD Patient on Hemodialysis

C

Chittagong Medical College

Status

Enrolling

Conditions

Chronic Kidney Disease Requiring Hemodialysis

Treatments

Drug: Folic Acid 5 Mg Oral Tablet
Drug: Zinc Sulfate 50 Mg Tab

Study type

Interventional

Funder types

Other

Identifiers

NCT06847139
PG.2024/1072

Details and patient eligibility

About

Hyperhomocysteinemia is a well-recognized risk factor for accelerated cardiovascular events in hemodialysis patients. Hyperhomocysteinemia is common in individuals with chronic kidney disease (CKD). Zinc is a vital cofactor for homocysteine metabolism enzymes. Although numerous studies have demonstrated the efficacy of folic acid in hyperhomocysteinemia, zinc supplementation has the potential to reduce homocysteine levels in hemodialysis patients. Objective: To evaluate the effect of Zinc supplementation on hyperhomocysteinemia compared to that of folic acid in patients with chronic kidney disease on hemodialysis. Materials and Methods: This open-label randomized active-controlled trial will be conducted in the Department of Nephrology of Chittagong Medical College Hospital, Chattogram, Bangladesh, for one and a half years. A total of ninety CKD patients on maintenance hemodialysis will be included in the study. Patients will be randomly divided into two groups. The experimental group will be treated with zinc sulfate (50 mg elemental zinc/day) for six weeks in conjunction with conventional treatment for CKD. The Control group will receive folic acid (5mg/day) along with conventional medications for CKD. The primary outcome measure will be the change in the plasma homocysteine level after 6 weeks, while the other variables will include serum creatinine, eGFR, serum albumin and C-reactive protein (CRP) level. Adverse events and safety measures will also be recorded. The primary analysis will be an intention to treat analysis performed with SPSS-23. Data from previous studies indicate zinc supplementation can reduce homocysteine levels in CKD patients facilitating its metabolism. Additionally, the anti-inflammatory properties of zinc may facilitate homocysteine reduction. Moreover, zinc is crucial in various physiological processes, including immune function, protein synthesis, and wound healing. Further clinical trials are still needed to understand better the safety and efficacy of zinc supplementation in CKD patients.

Enrollment

90 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

    1. Age ≥18 years 2. Patient with chronic kidney disease on HD for ≥ 3 months 3. Plasma homocysteine level > 15μmol/L

Exclusion criteria

  1. Acute illness at the time of inclusion.

  2. Diagnosed case of malabsorption

  3. Planned major surgery

  4. Renal transplantation

  5. Receiving zinc or folic acid supplementation within the previous month from enrollment.

  6. Concomitant use of vitamin B 12 supplementation(6 days), corticosteroid (18-36 hour), anti folate or cytotoxic drugs, quinolones, tetracyclines, bisphosphonates.

  7. Known hypersensitivity to zinc or folic acid.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

90 participants in 2 patient groups

patient getting zinc sulfate
Experimental group
Description:
patient will get zinc sulfate 50 mg daily
Treatment:
Drug: Zinc Sulfate 50 Mg Tab
patient getting folic acid
Active Comparator group
Description:
patient will get folic acid 5 mg
Treatment:
Drug: Folic Acid 5 Mg Oral Tablet

Trial contacts and locations

1

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Central trial contact

MD ZAKWAN ULLAH

Data sourced from clinicaltrials.gov

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