drugset / Trial / NCT00274586

Headache Study to Compare Aggrenox Full Dose and Reduced Dose

NCT00274586

Phase 3 Completed 100 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

Tolerability of a four weeks treatment with Aggrenox® modified release capsules b.i.d, compared to reduced dose during the first two weeks of treatment in a double-blind, randomized controlled parallel group comparison trial among Taiwanese patients with previous TIA's or ischemic stroke.To monitor frequency and intensity of headaches and other safety parameters among Taiwanese patients with previous TIA's or ischemic stroke given Aggrenox using a titration scheme or not

Timeline

Start
2002-09
Primary completion
2003-04
Completion
2003-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Aggrenox Unknown

Indications