Trial Condition(s):

Dysmenorrhea

Study to compare the analgesic efficacy and safety of Naproxen Sodium and Ibuprofen for the treatment of dysmenorrhea

Bayer Identifier:

Trial_CC-00138

ClinicalTrials.gov Identifier:

Not Available

EudraCT Number:

Not Available

Study Completed

Trial Purpose

Please see attached Study Results Summary below.

Inclusion Criteria
No Inclusion Criteria Available
Exclusion Criteria
No Exclusion Criteria Available

Trial Summary

Enrollment Goal
79
Trial Dates
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Phase
3
Could I receive a placebo?
No
Products
Aleve (Naproxen Sodium, BAY117031)
Accepts Healthy Volunteers
N/A

Where to Participate

Locations
Status
LocationsStatus

For details, please refer to trial results

Additional Information