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Research and Effect Evaluation on the Application of Precise Liquid Collection Device in Liquid Management of Hysteroscopic Surgery

Research and Effect Evaluation on the Application of Precise Liquid Collection Device in Liquid Management of Hysteroscopic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101460
Enrollment
Unknown
Registered
2025-04-25
Start date
2025-05-05
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Hysteroscopic eurgery

Interventions

Experimental group:Using precise liquid collection devices for collection
Control group:Collecting hysteroscopic perfusion fluid using the original perfusion fluid collection method

Sponsors

Lishui People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients admitted for hysteroscopy surgery during the project research period

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, brain, kidney and other organic lesions; 2. Patients who temporarily change the surgical method during hysteroscopic surgery; 3. Patients who are expected to use <=1000ml of perfusion solution required for surgery before surgery.

Design outcomes

Primary

MeasureTime frame
Collection rate of perfusion fluid;—

Secondary

MeasureTime frame
The average time for operating room staff to organize the operating room;Incidence of TURP syndrome;Satisfaction of surgeons and nurses;Fluid Leakage Volume;—

Countries

China

Contacts

Public ContactYing Yongli

Lishui People's Hospital

375299582@qq.com+86 189 5709 2669

Outcome results

None listed

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