Treatment of Primary Menstrual Pain With Kanion Capsule

Treatment of Primary Dysmenorrhea With Kanion Capsule (GF) A Randomized, Double-blind, Placebo-controlled, Repeated-Dose and Multi-Center Clinical Phase II Trial

Status

Completed

Phases

Phase 2

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00523146

Enrollment

Unknown

Registered

2007-08-31

Start date

2007-04-30

Completion date

2009-02-28

Last updated

2010-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Dysmenorrhea

Keywords

primary dysmenorrhea, Herbal remedy

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.

Interventions

DRUGKanion Capsule

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender

FEMALE

Age

18 Years to 45 Years

Healthy volunteers

Inclusion criteria

* primary dysmenorrhea

Exclusion criteria

* secondary dysmenorrhea

Design outcomes

Primary

Measure	Time frame
pain reduction	6 months

Secondary

Measure	Time frame
accompanying symptoms improvement	6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026