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Primary Dysmenorrhoea Treated by Gegen Decoction: A Randomized, Double Blind, Placebo Control Trial

Primary Dysmenorrhoea Treated by Gegen Decoction: A Randomized, Double Blind, Placebo Control Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002847
Enrollment
Unknown
Registered
2012-10-13
Start date
2011-10-31
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Primary Dysmenorrhea

Interventions

GGT group:Gegen decoction
Control group:Placebo

Sponsors

The Affiliated Zhongda Hospital of Southeast University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1. Female, 18-30 years old; 2. Primary Dysmenorrhea was diagnosed, lasting for half a year at least; 3. Pain intensity is more than 4 by method of visual analogue scale; 4. Mense circle between 23-35 days; 5. Secondary Dysmenorrhea is excluded by sonography; 6. No severe diseases of liver, kidney, heart and blood system; 7. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who is taking prophylactic, using contraceptive, want to be pregnant within half a year, and patients who has been pregnent or in feeding period; 2. Secondry Dysmenorrhea was proved by examination; 3. Patients with serious diseases of circulation, kidney, liver and blood system; 4. Patients with digestive ulcer; 5. Drugs/alcohol abuse; 6. Patients who is incompetent to judge; 7. Bad compliance or abnormal mental status; 8. Hypersensitive to NSAIDS or sulfa; 9. Other causes.

Design outcomes

Primary

MeasureTime frame
Pain Visual Analogue Scale;

Secondary

MeasureTime frame
The McGill Pain Questionnaire;Menstrual Distress Questionnair;

Countries

China

Contacts

Public ContactWang Changsong
kingdoc@126.com+86 13645188512

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026