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Construction and verification of a continuous perfusion ex vivo organ training model for minimally invasive basic skills in gynecology

Construction and validation of a continuous perfusion ex vivo organ training model for basic gynecological minimally invasive skills

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094776
Enrollment
Unknown
Registered
2024-12-27
Start date
2025-01-05
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Uterine fibroids

Interventions

SMTG group:Complete 15 rounds of CPTM training
MMTG group:DBTM training in the first half and CPTM training in the second half.
FLSTGgroup:The first round of CPTM operation LM is conducted to record initial performance, learn the five manual skill tasks required by the FLS program and pass the assessment, and then the CPTM ope
Intermediate group:One laparoscopic myomectomy was performed on CPTM.
Expert group :One laparoscopic myomectomy was performed on CPTM.

Sponsors

Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
23 Years to 40 Years

Inclusion criteria

Inclusion criteria: Primary group: Residents with no practical experience in laparoscopic surgery (regular training/professional and master's students) Intermediate group: Laparoscopic myomectomy is required to be performed within 10 times Expert group: Required to perform more than 75 laparoscopic myomectomy as the chief surgeon

Exclusion criteria

Exclusion criteria: Visual acuity above 600 degrees (for normal use of the eye tracker device)

Design outcomes

Primary

MeasureTime frame
Operating time;Intraoperative blood loss and intraoperative blood loss within 5 minutes after surgery;Suture maximum gap length and total tear length;—

Countries

China

Contacts

Public ContactJianyi Li

Department of Anatomy, School of Basic Medical Sciences, Southern Medical University

wuxili74@126.com+86 186 6500 0205

Outcome results

None listed

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