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

EU CT 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

Trial Dates

December1995

March1996

Phase

Could I receive a placebo?

Products

Aleve (Naproxen Sodium, BAY117031)

Accepts Healthy Volunteers

N/A

Where to Participate

Locations

Locations

Dysmenorrhea

Bayer Identifier:

ClinicalTrials.gov Identifier:

EudraCT Number:

EU CT Number:

Trial Purpose

Key Participation Requirements

sex

age

16 Years

No Limit

Inclusion Criteria

Exclusion Criteria

Inclusion Criteria

Exclusion Criteria

Trial Summary

Enrollment Goal

Trial Dates

Phase

Could I receive a placebo?

Products

Accepts Healthy Volunteers

Where to Participate

For details, please refer to trial results

Additional Information