Skip to content

Clinical Analysis of the Modified Balloon-Expansion Connection Technique in Hysteroscopic Surgery

Clinical Efficacy Analysis of a Modified Peristaltic Hysteroscopic Distension Pump Connection Method in Hysteroscopic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112415
Enrollment
Unknown
Registered
2025-11-13
Start date
2025-11-15
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Patients scheduled for hysteroscopic procedures in the operating theatre for uterine cavity disorders

Interventions

Control group (conventional connection method):NA
Observation group (modified connection method):NA

Sponsors

The international peace maternity and child health hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients scheduled for elective hysteroscopic surgery; 2.Age: 18 to 65 years old; 3.Body Mass Index (BMI) 18–30 kg/m²;

Exclusion criteria

Exclusion criteria: 1.? Patients with diabetes mellitus; 2.? Patients with a history of sterilisation surgery; 3.? Patients with malignant uterine lesions; 4.? Patients with acute pelvic inflammatory disease or acute exacerbation of chronic pelvic inflammatory disease;

Design outcomes

Primary

MeasureTime frame
Hysteroscopic examination duration (minutes);Duration of surgery (minutes);Negative deficit in perfusion medium (ml);Surgeon's assessment of surgical field clarity (5-point scale);

Countries

China

Contacts

Public ContactShiping Cheng

The international peace maternity and child health hospital

1310370267@qq.com+86 21 6407 0434

Outcome results

None listed

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