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Construction and clinical application of a predictive model for postoperative pregnancy outcomes in deep infiltrating endometriosis

Construction and clinical application of a predictive model for postoperative pregnancy outcomes in deep infiltrating endometriosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089375
Enrollment
Unknown
Registered
2024-09-06
Start date
2024-09-07
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

deep infiltrating endometriosis

Interventions

Pregnancy group:Pregnant patients after DIE surgery
Non-pregnancy group:Non-pregnant patients after DIE surgery
Prospective research group:Prospective inclusion and follow-up of postoperative pregnancy outcomes in patients undergoing DIE surgery

Sponsors

Obstetrics and Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.1 Inclusion criteria for retrospective studies: 1) From January 2009 to January 2022, DIE patients underwent surgical treatment with pathological diagnosis of DIE in the Obstetrics and Gynecology Hospital of Fudan University, ; 2) Complete medical history records (basic information, surgical and medical records) and pathological data; 3) Preoperative specialized examination records: vagino-recto-abdominal examination; Complete imaging examinations such as B-ultrasound and MRI before surgery, and have complete imaging data; 4) Telephone follow-up successful, recording pregnancy outcomes. 1.2 Inclusion criteria for prospective studies: 1) Prospective collection of patients with clinical diagnosis of DIE combined with infertility; 2) Age range: 18-45 years old; 3) Intending to be hospitalized for DIE surgical treatment, with complete medical history information available; 5) Intraoperative histopathological specimens can be obtained, and postoperative pathology confirms the DIE subtype; 6) Accepting regular long-term follow-up 7) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Refuse long-term follow-up; 2) Merging gynecological malignant tumors or other gynecological hormone dependent diseases; 3) Incomplete medical history data, inability to cooperate with gynecological specialist examinations, or lack of imaging data, serum biomarker reports, etc; 4) Postoperative pathological diagnosis didn't indicate endometriosis. 5) Male with abnormal semen

Design outcomes

Primary

MeasureTime frame
pregnant rate;Safety index;

Secondary

MeasureTime frame
recurrence rate;surgery complications;Health economics;EHP-30;FSFI;Sex hormone levels;

Countries

China

Contacts

Public ContactZhang Ning

Obstetrics and Gynecology Hospital of Fudan University

347205277@hotmail.com+86 188 1821 0746

Outcome results

None listed

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