Skip to content

Clinical study of Wenjing decoction combined with dydrogesterone in the treatment of pelvic pain with deep infiltrating endometriosis

Integrated Chinese and Western Obstetrics and Gynecology

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2200005849
Enrollment
Unknown
Registered
2022-04-12
Start date
2022-04-12
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Endometriosis

Interventions

Observation group:Wenjing Decoction + Dydrogesterone
Control group :Dydrogesterone
Placebo group : Placebo

Sponsors

the Third Affiliated Hospital of Zhejiang Chinese University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: a Complaints of pelvic pain, with a VAS score of 4 or above; b Meet the diagnostic criteria for deep infiltrating endometriosis; c Comply with the syndrome of cold coagulation and blood stasis; d Female, between 18-45 years old; menstrual cycle is regular, the menstrual cycle is 21-35 days; e Those who have not taken hormone drugs in the past 3 months; f There is no pregnancy plan during the medication period, and contraceptive contraception is used; g Those who voluntarily participate in this trial and have signed an informed consent form.

Exclusion criteria

Exclusion criteria: a Combined with adenomyosis, pelvic inflammatory mass, and endometriotic cyst diameter = 4cm; b DIE The lesion penetrates the rectal mucosa and bladder mucosa, and the lesion compresses the ureter to cause transfusion. Urinary tube dilation, hydronephrosis; c Patients with malignant tumors of reproductive organs or other malignant tumors; d People with serious or mental illnesses such as cardiovascular, cerebrovascular, liver, kidney or hematopoietic system; e Patients with endometriosis who underwent surgical treatment within 3 months before enrollment; f Patients planning pregnancy, pregnancy or lactation in the past 3 months.

Design outcomes

Primary

MeasureTime frame
VAS score;

Secondary

MeasureTime frame
Lesion size;EHP-5;Serum CA125 level;Serum CA125 level;

Countries

China

Contacts

Public ContactJIANG Yanjiao
1403699722@qq.com13185719869

Outcome results

None listed

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