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A prospective cohort study of pharmacological versus surgical treatment of intestinal endometriosis

A prospective cohort study of pharmacological versus surgical treatment of intestinal endometriosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074842
Enrollment
Unknown
Registered
2023-08-17
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Endometriosis

Interventions

Medicine group (Endometriosis-related medicine):None
Surgery Group (Surgery ± Postsurgical Medicine):None

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Informed consent has been signed (2) Women of childbearing age: 20-45 years old (3) Clinical diagnosis (symptoms, gynecological examination, ultrasound and/or MRI) or biopsy pathological diagnosis (4) Exclude contraindications to estrogen and progesterone drugs

Exclusion criteria

Exclusion criteria: (1) Patients who participate in other interventional research projects in addition to routine clinical diagnosis and treatment (2) Patients with poor living conditions, incapacitation or loss of consciousness. (3) The investigator believes that it is not suitable to participate in this study. (4) Patients with complete obstructive intestinal heterogeneity. (5) Previous history of severe liver disease (6) Patients with combined or diagnosed malignant tumors (7) Patients with other intestinal diseases (such as inflammatory bowel disease, familial adenomatous polyposis, etc.) or patients with a history of intestinal surgery (8) Combined with diseases that may affect intestinal function or taking related drugs (such as aminosalicylic acid preparations, thiopurines, glucocorticoids, etc.) within 3 months;

Design outcomes

Primary

MeasureTime frame
Health-related quality of life;patient global impression of change;Direct economic costs;

Secondary

MeasureTime frame
Efficacy;Recurrence;Pain (Dysmenorrhea, dyspareunia, non-cyclic pelvic pain);gastrointestinal quality of life;Urinary symptoms;

Countries

China

Contacts

Public ContactYi Dai

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

jacquedai@vip.sina.com+86 186 1102 7788

Outcome results

None listed

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