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A clinical trial to study the effects of two drugs,ZYH1 and Rosiglitazone in diabetic patients with high lipid levels.[Prospective Randomised Efficacy and Safety of Saroglitazar (PRESS II)]

Phase 2
Completed
Conditions
Hyperlipidemia, unspecified,
Registration Number
CTRI/2010/091/000165
Lead Sponsor
Cadila Healthcare Limited
Brief Summary

This was a a 12 week, randomized, double blind, parallel group, prospective, dose ranging, and comparative study of ZYH1 with an open Rosiglitazone arm to evaluate the efficacy and safety of oral 0.5, 1, 2 and 4mg ZYH1 as compared to the highest recommended dose of Rosiglitazone ( 8/16 mg daily) on lipid profile and glycemic control in patients suffering from dyslipidemia with diabetes mellitus.The Primary efficacy endpoints: 1.Triglyceride 2.Low density Lipoproteins ( LDL) cholesterol, 3.Very low density lipoprotein (VLDL) cholesterol, 4.HDL cholesterol and 5.Fasting Glucose. The Secondary efficacy endpoints: 1.HbA1C, 2.Insulin and 3.C-Reactive protein(CRP) The efficacy variables were assessed as percent change at the end of treatment phase i.e., Week 12, as compared to start of treatment phase i.e., Week 0

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
30
Inclusion Criteria
  • 1.Patients of either sex > or =18 years of age.2.Established diagnosis of dyslipidemia with BMI 23-42kg/m2 with fasting triglyceride level > or = 150mg/dL.
  • 3.Established diagnosis of Type 2 Diabetes Mellitus with Fasting Blood glucose > or = 126mg/dL (According to American Diabetes Association) with or without on treatment with other hypoglycemic drugs.4.Normal routine hematological and biochemical test results.
  • 5.Informed consent of the patient / relative.
Exclusion Criteria
  • 1.Hypersensitivity to sulpha drugs or ZYH1.
  • 2.Pregnancy & Lactation.
  • 3.Patients with active liver disease or hepatic dysfunction indicated by AST or ALT levels  2.5 times the upper limit of normal.
  • 4.Patients with history of myopathy or evidence of active muscle disease.
  • 5.Haemoglobin less than 11mg% 6.Patients on concomitant medications known to affect lipid levels and glucose levels and do not want to enter in wash out period.
  • 7.Patients with any other serious concurrent illness or malignancy.
  • 8.Presence or history of gallstone.
  • 9.Patients with continuing history of alcohol and / or drug abuse.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary efficacy endpoints: 1.Triglyceride 2.Low density Lipoproteins ( LDL) cholesterol, 3.Very low density lipoprotein (VLDL) cholesterol, 4.HDL cholesterol and 5.Fasting Glucose.From baseline, visit 2(Week 0)to visit 8 (Week 12)
Secondary Outcome Measures
NameTimeMethod
Secondary efficacy endpoints: 1.HbA1C, 2.Insulin and 3.C-Reactive protein(CRP)From baseline, visit 2 (Week 0)to visit 8 (Week 12)

Trial Locations

Locations (2)

Institute of Postgraduate Medical Education & Research (IPGMER)

🇮🇳

Kolkata, WEST BENGAL, India

Post-Graduate Institute of Medical Education & Research (PGIMER)

🇮🇳

Chandigarh, CHANDIGARH, India

Institute of Postgraduate Medical Education & Research (IPGMER)
🇮🇳Kolkata, WEST BENGAL, India
Dr. Satinath Mukherjee
Principal investigator
09830027985
satinath.mukhopadhyay@gmail.com

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