Treatment of Primary Menstrual Pain With Kanion Capsule

Phase 2

Completed

• Conditions: Primary Dysmenorrhea

• Registration Number: NCT00523146
• Lead Sponsor: Lianyungang Kanion Group, Ltd.

Brief Summary

The objectives of this clinical trial are:

* To further study the safety of Kanion Capsule (GF) in primary dysmenorrhea subjects;

* To further evaluate the efficacy of GF in treatment of primary dysmenorrhea.

Detailed Description

Not available

Study Timeline

• Study Start: 2007-04
• Study First Submitted: 2007-08-29
• Study First Submitted QC: 2007-08-29
• Study First Posted: 2007-08-31
• Primary Completion: 2008-12
• Study Completion: 2009-02
• Status Verified: 2010-02
• Last Update Submitted: 2010-02-02
• Last Update Posted: 2010-02-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

• primary dysmenorrhea

Exclusion Criteria

• secondary dysmenorrhea

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
pain reduction	6 months

Secondary Outcome Measures

Name	Time	Method
accompanying symptoms improvement	6 months

Trial Locations

Locations (1)

Mount Vernon Clinical Research, LLC; 🇺🇸 Sandy Springs, Georgia, United States