RecruitingPhase 3NCT04666714

Efficacy and Safety of Praga Formulation in the Treatment of Neuropathic Pain

National, Multicentre, Randomized, Double-blind, Double-dummy Phase III Clinical Trial to Evaluate the Efficacy and Safety of Praga Formulation in the Treatment of Neuropathic Pain


Sponsor

EMS

Enrollment

136 participants

Start Date

May 15, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate the efficacy and safety of Praga formulation in the treatment of neuropathic pain.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Placebo Praga formulation, Placebo Pregabalin 150mg, and others for people with neuropathic pain. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPraga formulation

Praga formulation tablet

OTHERPlacebo pregabalin 75mg

Placebo pregabalin 75mg tablet

OTHERPlacebo Pregabalin 150mg

Placebo Pregabalin 150mg tablet

DRUGPregabalin 75mg

Pregabalin 75mg tablet

DRUGPregabalin 150mg

Pregabalin 150mg tablet

OTHERPlacebo Praga formulation

Placebo Praga formulation tablet


Locations(1)

Allegisa

Campinas, São Paulo, Brazil

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NCT04666714


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