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Safety and feasibility of total laparoscopic radical hysterectomy for patients with cervical cancer

Safety and feasibility of total laparoscopic radical hysterectomy for patients with cervical cancer - Safety and feasibility of total laparoscopic radical hysterectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024421
Enrollment
25
Registered
2016-10-15
Start date
2016-10-01
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

Interventions

Laparoscopic raadical hysterectomy

Sponsors

Ehime University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) an age of 20 - 75 years 2) the presence of histologically-proven cervical cancer 3) an International Federation of Gynecology and Obstetrics (FIGO) stage of IA2, IB1, or IIA1 4) Those with adequate organ function 5) Performance status (PS) from 0 to 2 6) Those who have given written informed consent

Exclusion criteria

Exclusion criteria: 1) Patients who have recurrence of cervical cancer 2) Those with previous laparotomy (excluded with appendectomy, cesarean section and surgery for ovarian tumor) or previous radiotherapy of abdomen 3) Those with concomitant active malignancy 4) Those with serious complication 5) Those who are pregnant or suspected to be pregnant 6) Body Mass Index of 30 or greater 7) Those with diagnosis of uterine cervical myoma with ultrasound scanning 8) Patients participating other clinical studies within twelve months. 9) Those who are inadequate to be enrolled in the protocol study by the investigator

Design outcomes

Primary

MeasureTime frame
Pathological evaluation of curability with resected specimen and the 3-year relapse-free survival.

Countries

Japan

Contacts

Public ContactToru Fujioka

Ehime University, Graduate School of Medicine Department of Obstetrics and Gynecology

fujioka@m.ehime-u.ac.jp089-960-5379

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026