Feasibility study to evaluate efficacy and safety of laparoscopic radical histerectomy in Kanazawa University Hospital.

Feasibility study to evaluate efficacy and safety of laparoscopic radical histerectomy in Kanazawa University Hospital. - Feasibility study to evaluate efficacy and safety of laparoscopic radical histerectomy in Kanazawa University Hospital.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000021014

Enrollment

Registered

2016-02-15

Start date

2016-02-18

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Cervical cancer stage IA2,IB1 and IIA1

Interventions

None listed

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Patient is pathologically diagnosed as cervical cancer. Patient is clinically staged as IA2,IB1 or IIA1. We need to obtain written informed consent by the patient. Patient condition is acceptable for general anesthesia.

Exclusion criteria

Exclusion criteria: Patient has psycological disorder unacceptable to participate in the trial. When the physician determined the patient is inadequate for the trial

Design outcomes

Primary

Measure	Time frame
Frequency of perioperative complication(beyond grade2)	—

Countries

Japan

Contacts

Public ContactYasunari Mizumoto

Kanazawa Univ. Hospital Dept. of OB/GYN

yas1025@med.kanazawa-u.ac.jp076-265-2425

Outcome results