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Multicentre assessment of the quality of uterine reconstruction after fertility preservation surgery for diffuse adenomyosis

Multicentre assessment of the quality of uterine reconstruction after fertility preservation surgery for diffuse adenomyosis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078234
Enrollment
Unknown
Registered
2023-12-01
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

adenomyosis

Interventions

Case series:NA

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1) The patients after PUSH surgery were pathologically confirmed as adenomyosis, with severe dysmenorrhea before surgery, visual blur score =7, and need analgesic drugs; Diffuse lesions with a uterus = 70 days gestational size (volume =100cm3) involving more than 80% of the anterior and/or posterior wall muscles, or a thickened single layer of more than 6cm. 2) Age 20-45. 3) Fully informed and voluntary consent to participate in this study.

Exclusion criteria

Exclusion criteria: 1) No study was included if any of the above inclusion criteria were not met. 2) The subject is unable or unwilling to complete the study procedure.

Design outcomes

Primary

MeasureTime frame
Muscle filling defect volume;

Secondary

MeasureTime frame
Postoperative pain improvement;Menstrual changes;The incidence of perioperative complications;

Countries

China

Contacts

Public ContactQicai Hu

Peking University Shenzhen Hospital

aa13255599860@126.com+86 182 0767 9259

Outcome results

None listed

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