Design and development of uterine device for laparoscopic radical resection of cervical cancer

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100042249

Enrollment

Unknown

Registered

2021-01-17

Start date

2021-01-18

Completion date

Unknown

Last updated

2021-04-19

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

Conditions

Obstetrical and gynecological devices related to injury or injury: surgical instruments, materials, or devices

Interventions

Test group:Half abandon the use of balloon uterine lifting device

control group:Nil

Eligibility

Sex/Gender

Female

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) patients who need to use uterine lifting device for laparoscopic surgery; (2) agree to participate in this study.

Exclusion criteria

Exclusion criteria: (1) the disease is not allowed to proceed with this researcher; (2) the surgeon thinks that other reasons are not suitable to participate in this researcher.

Design outcomes

Primary

Measure	Time frame
With or without uterine injury;	—

Countries

China

Contacts

Public ContactKangya Yang

Obstetrics and Gynecology Hospital affiliated to Medical College of Zhejiang University

yangky@zju.edu.cn+86 18258834813

Outcome results

None listed

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