Effect on Primary Dysmenorrhea

Status Completed

Clinical Trial Summary

To investigate the potential benefits of a new oral contraceptive (SH T00658ID) on alleviating complaints of dysmenorrhea associated with oral contraceptive use.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00909857
Study type	Interventional
Source	Bayer
Contact
Status	Completed
Phase	Phase 3
Start date	April 2009
Completion date	November 2010

View Details

See also
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