ITMCTR2000003429
Not yet recruiting
Phase 1
A randomized controlled study on the treatment of primary dysmenorrhea with heat burning blood stasis by Guizhi Fuling Wan
Yichang Second People's Hospital0 sitesTBD
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Yichang Second People's Hospital
- Status
- Not yet recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Those who meet the following 7 items can be included in the study. If there is any inconformity, the patient cannot enter the study
- •1\. Patients aged 16\-30 years;
- •2\. To diagnose patients with primary dysmenorrhea according to the consensus guideline of primary dysmenorrhea;
- •3\. No parturient;
- •4\. Self described pain duration: from 6 months to 15 years;
- •5\. Patients with an average pain intensity of 40 or more (VAS by 100 mm visual analogue scale) and at least three consecutive menstrual cycles;
- •6\. Patients with syndrome of heat burning and blood stasis;
- •7\. The informed consent shall be signed by the patient himself or by his immediate relatives.
Exclusion Criteria
- •Patients cannot enter the study if any of the following are met:
- •1\. Patients who can not complete the treatment plan of this study within half a year;
- •2\. Patients with secondary dysmenorrhea (such as endometriosis or adenomyosis);
- •3\. Patients with irregular menstrual cycle (beyond the typical range of 21\-35 days);
- •4\. Women with pregnancy plan in the past half year;
- •5\. Patients with mental disorders and mental disorders who can not cooperate with the questionnaire survey;
- •6\. Patients with serious cardiovascular disease, liver and kidney function damage, psychological disease or life\-threatening situation;
- •7\. Patients who are using analgesics;
- •8\. Patients who have participated in or are participating in other clinical trials.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Not yet recruiting
Early Phase 1
A randomized controlled study on the treatment of androgen alopecia caused by spleen deficiency and dampness in combination with Qushi Jianfa Decoction for internal administration.Androgenic alopeciaITMCTR2024000172Beijing Traditional Chinese Medicine Hospital Affiliated to Capital Medical University
Not yet recruiting
Phase 1
A randomized controlled study on the treatment of insomnia after stroke by He's acupuncture-moxibustion three removing obstruction methodsinsomnia after strokeITMCTR2200006770Beijing Hospital of Traditional Chinese Medicine Shunyi Hospital
Completed
Early Phase 1
A randomized controlled study on the treatment of severe acute pancreatitis with intraperitoneal hypertension through nasogastric nutrition tube administration of GansuiITMCTR2024000034Guangdong Provincial Hospital of Chinese Medicine
Not yet recruiting
Phase 1
A randomized controlled study for the treatment of depression by regulating circadian rhythm with Sini SaITMCTR1900002301Shaanxi Traditional Chinese Medicine Hospital
Completed
Not Applicable
A Randomised, Prospective Study of the Treatment of Superficial Partial-Thickness Burns:AWBAT (Trademark) vs. Biobrane (Registered Trademark)Superficial partial-thickness burnsSurgery - Other surgeryACTRN12609000765224Royal Adelaide Hospital60