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Clinical efficacy of different surgical methods in patients with adenomyosis

clinical efficacy of different surgical methods in patients with adenomyosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000038934
Enrollment
Unknown
Registered
2020-10-10
Start date
2020-10-30
Completion date
Unknown
Last updated
2021-07-05

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

Conditions

adenomyosis

Interventions

radical operation vs. non radical operation:Nil

Sponsors

Qilu hospital, Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients who underwent adenomyosis-related surgery in the investigator's hospital from 2009/01/01 to 2019/12/31, and received follow-up medication.

Exclusion criteria

Exclusion criteria: Unwilling to participate in clinical trials and follow-up.

Design outcomes

Primary

MeasureTime frame
Pain before and after surgery;—

Secondary

MeasureTime frame
Hemoglobin;Tumor marker (CA-125);Ultrasound image tracking;pregnancy rate for the adenomyosis women of childbearing age;—

Countries

China

Contacts

Public ContactLijie Wang

Department of Obstetrics and Gynecology, Qilu Hospital, Shandong University

wangljie@hotmail.com+86 18560081857

Outcome results

None listed

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