Skip to content

Study on perioperative coagulation status of adenomyosis - Prospective observational study

Study on perioperative coagulation status of adenomyosis - Prospective observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114741
Enrollment
Unknown
Registered
2025-12-17
Start date
2025-12-31
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Adenomyosis

Interventions

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Adenomyosis group: Age 30-52 years old, dysmenorrhea and/or menorrhagia, color ultrasound and/or magnetic resonance imaging suggested adenomyosis, hemoglobin greater than 60g/L; 2.Uterine fibroid group: age 30-52 years old, color ultrasound and/or magnetic resonance imaging showed uterine fibroid, hemoglobin greater than 60g/L.

Exclusion criteria

Exclusion criteria: 1. Combined with endometriosis such as chocolate cysts; 2. Combined with other systemic diseases such as diabetes, hypertension, hyperlipidemia, autoimmune diseases, etc.; 3. Combined with other diseases affecting coagulation function; 4. Patients who have received blood transfusions; 5. Recent use of hormone therapy.

Design outcomes

Primary

MeasureTime frame
Coagulation Function Analysis;

Secondary

MeasureTime frame
Platelet;

Countries

China

Contacts

Public ContactWu Qing

Zhejiang Provincial People's Hospital

okwq31@163.com+86 151 6717 0568

Outcome results

None listed

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