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
| Type | Name | Description |
|---|---|---|
| DRUG | Meloxicam 7.5 mg | |
| DRUG | Meloxicam 15 mg | |
| DRUG | Mefenamic acid 500 mg | |
| DRUG | Placebo matching 7.5 mg meloxicam | |
| DRUG | Placebo matching 15 mg meloxicam | |
| DRUG | Placebo 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.