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Clinical Trial Summary

The purpose of this study is to evaluate the non-inferiority clinical efficacy of two different associations of drugs in the treatment of patients diagnosed with tensional-type headache in accordance with International Headache Society guidelines.


Clinical Trial Description

- Open-label, non-inferiority, prospective, parallel group, intent to treat trial. - Experiment duration: 56 days. - 04 visits (days -7, 0, 28 and 56). - Efficacy will be evaluated for 10 episodes of tension-type headache. - Adverse events evaluation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01408069
Study type Interventional
Source EMS
Contact
Status Withdrawn
Phase Phase 3