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Clinical Trial Summary

The purpose of this study is to assess the efficacy and tolerability of orally administered dimiracetam for 10 weeks to AIDS patients under treatment with antiretroviral agents presenting a disease and /or treatment related neuropathic pain.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01444690
Study type Interventional
Source Neurotune AG
Contact Rugerro Fariello, MD
Phone +41-91-6056542
Email ruggero.fariello@neurotune.com
Status Not yet recruiting
Phase Phase 2
Start date January 2012
Completion date January 2013

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