Study on the application effect of modified surgical drape in gynecological lithotomy

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300068493

Enrollment

Unknown

Registered

2023-02-21

Start date

2023-03-01

Completion date

Unknown

Last updated

2023-05-22

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

Conditions

gynecological lithotomy

Interventions

Experimental group:Improved surgical drape

Control group:normal surgical drape

Eligibility

Sex/Gender

Female

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: ? Patients aged 18-60 years old ? The patient has undergone gynecological surgery in advance, and the surgical position is the lithotomy position ? Patients volunteered to participate in this study ? The operation time of the patient is more than 1 hour

Exclusion criteria

Exclusion criteria: ? Patients undergoing gynecological surgery temporarily converted from the supine position to the lithotomy position during the operation ? Emergency admission patients ? The patient is complicated with other serious diseases and cannot tolerate the lithotomy position

Design outcomes

Primary

Measure	Time frame
Pre-operative bed unit preparation time;Time to establish sterile area of perineal area;Degree of wetness in sterile area;The patient's sacrococcygeal skin condition;	—

Countries

China

Contacts

Public ContactZhang Chen

Peking University First Hospital

LX89617@126.com13699128176

Outcome results

None listed

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