Clinical Trials Directory

Trials / Completed

CompletedNCT02183025

Efficacy and Safety Study of Meloxicam Versus Mefenamic Acid in Patients With Dysmenorrhea

Double Blind Study to Evaluate Efficacy and Safety of Meloxicam 7.5 mg and 15 mg Versus Mefenamic Acid 1500 mg in the Treatment of Dysmenorrhea

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
337 (actual)
Sponsor
Boehringer Ingelheim · Industry
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

To access the efficacy and safety of Meloxicam 7.5 mg and 15 mg once daily compared with Mefenamic acid 500 mg t.i.d. over a treatment period of 3-5 days, during an observation period of 3 menstrual cycles, for the symptomatic relief of primary dysmenorrhea

Conditions

Interventions

TypeNameDescription
DRUGMeloxicam 7.5 mg
DRUGMeloxicam 15 mg
DRUGMefenamic acid 500 mg
DRUGPlacebo matching 7.5 mg meloxicam
DRUGPlacebo matching 15 mg meloxicam
DRUGPlacebo matching 500 mg mefenamic acid

Timeline

Start date
1998-01-01
Primary completion
1999-04-01
First posted
2014-07-08
Last updated
2018-08-31

Source: ClinicalTrials.gov record NCT02183025. Inclusion in this directory is not an endorsement.