drugset / Trial / NCT00328601

Assessment of Efficacy and Safety of Thioctic Acid in the Oral Treatment of Symptomatic Diabetic Neuropathy (SYDNEY 2)

NCT00328601

Phase 3 Completed 170 enrolled MEDA Pharma GmbH & Co. KG
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of the trial is to determine the optimal dose of orally (tablet) administered thioctic acid in the treatment of symptoms of diabetic polyneuropathy (dPNP). It is expected that at least one of the three dosages to be tested (600, 1200, or 1800 mg tablets) of orally administered thioctic acid improves the symptoms of dPNP as compared to placebo. Secondary objectives are evaluations of other variables pertinent to dPNP, safety, and tolerability.

Timeline

Start
2005-02
Primary completion
Completion
2005-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Thioctic Acid Unknown 600 mg Oral
Subject Thioctic Acid Unknown 1200 mg Oral
Subject Thioctic Acid Unknown 1800 mg Oral