Study on the method and effect of ultrasound-guided artificial pelvic isolation fluid during transabdominal puncture and sclerosis of ovarian endometriosis cyst

Study on the method and effect of ultrasound-guided artificial pelvic isolation fluid during sclerosis of ovarian endometriosis cyst

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000039380

Enrollment

Unknown

Registered

2020-10-25

Start date

2020-10-18

Completion date

Unknown

Last updated

2021-02-01

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

Conditions

Ovarian endometriosis cyst

Interventions

experimental group:Use artificial pelvic fluid isolation technology

control group:without using artificial pelvic fluid isolation technology

Eligibility

Sex/Gender

Female

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients with OEC (>= 4 cm); 2. Patients evaluated by ultrasound and MRI before operation; 3. Patients have the intention of ultrasound-guided puncture sclerotherapy; 4. The patients who received cytological examination after operation.

Exclusion criteria

Exclusion criteria: 1. Patients with malignant signs of ovarian cyst suspected by ultrasound or MRI; 2. Patients with abnormal coagulation function; 3. Patients with infectious lesions on the puncture path; 4. Patients with other major organ dysfunction or mental disorders; 5. Patients allergic to alcohol drugs.

Design outcomes

Primary

Measure	Time frame
Patient comfort;Intraoperative pain VAS score;	—

Countries

China

Contacts

Public ContactXu Mingmin

Zhejiang Veteran Hospital

mingminxu@126.com+86 13511300148

Outcome results

None listed

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