Overview
Study to Assess the Effect of Zinc in Atorvastatin Treated Hyperlipidemic Patients
Status:
Recruiting
Recruiting
Trial end date:
2022-07-10
2022-07-10
Target enrollment:
0
0
Participant gender:
All
All
Summary
This study was 8 weeks randomized, double-blind, placebo-controlled trial to assess the effect of zinc in Atorvastatin treated hyperlipidemic 92 patients. Participants were assessed at baseline, and 8 weeks. Subjects were randomized to receive either atorvastatin+placebo in one arm or atorvastatin +zinc 30mg tablet in another arm daily for 8 weeks. The outcome was the measure of fasting lipid profile, sgpt, serum creatinine at baseline and after 8 weeks following the intervention.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Bangabandhu Sheikh Mujib Medical University, Dhaka, BangladeshTreatments:
Zinc Sulfate
Criteria
Inclusion Criteria:- Age: 18 to 75 years
- Sex: both male and female
- Hyperlipidemic patients suffering from ischemic heart disease, diabetes mellitus,
hypertension.
- A person can develop hyperlipidemia if they have one or a combination of the
following: Diagnostic criteria for dyslipidemic patients (NCEP ATP III guideline)
Total Cholesterol > 240 mg/dl LDL-C > 100 mg/dl Triglyceride > 150 mg/dl HDL-C < 40
mg/dl
Exclusion Criteria:
- Patients with renal impairment.
- Patient with history of active liver disease (e.g. jaundice, hepatitis, cirrhosis)
- Patients having hypersensitivity to drugs.
- Patients with any systemic diseases or having serious infections or terminal illness
(e.g.-tuberculosis, HIV, malignant tumor)
- Pregnant woman
- lactating mother