drugset / Trial / NCT06558006

Safety and Efficacy Predimenol for Headache

NCT06558006 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a prospective, double-blind, placebo-controlled and randomized study aimed to obtain a description of the efficacy and safety of Predimenol in alleviating headache.

Timeline

Start
2024-06-19
Primary completion
2024-10-15
Completion
2024-10-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Predimenol Unknown 200 mg Oral
Subject Predimenol Unknown 400 mg Oral

Indications