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NCT00940251

Evaluation of Safety and Efficacy of Mersina, an Ayurvedic Formulation: A Double Blind, Placebo Controlled Study in Type 2 Diabetic Patients With Secondary Failure to Oral Drugs

Completed Phase 2 Last updated 14 July 2009
What this trial tests

Phase 2 trial testing Mersina in Antihyperglycemic Effect in Type 2 Diabetic Patients With Secondary Failure to Oral Hypoglycemic Agents in 26 participants. Completed in 1 November 2008.

Timeline
1 September 2008
Primary endpoint
1 October 2008
1 November 2008

Quick facts

Lead sponsorJyoti Clinical and Pathological Laboratory
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment26
Start date1 September 2008
Primary completion1 October 2008
Estimated completion1 November 2008
Sites1 location across India

Drugs / interventions tested

Conditions studied

Sponsor

Jyoti Clinical and Pathological Laboratory

Who can join

Adults 30 to 60, any sex, with Antihyperglycemic Effect in Type 2 Diabetic Patients With Secondary Failure to Oral Hypoglycemic Agents. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

To determine the safety and efficacy of an Ayurvedic formulation, Mersina in type 2 diabetic patients with secondary failure to oral hypoglycemic agents, a randomized double blind, single centre, study of 3 months duration was carried out.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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