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Study identifier: NCT05186493 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Laparoscopic Robot-assisted Pelvic Exenteration for Pelvic Primary and Recurrent Cancers

Condition: Locally Advanced Pelvic Cancer That Require Pelvic Exenteration  ·  Sponsor: Oslo University Hospital

PhaseNA
Planned participants40
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The Radium Hospital Oslo University Hospital Estimated date of first patient enrolled: 3rd quarter 2021 Anticipated recruitment period: 4 years Estimated date of last patient completed: 4th quarter 2025 Locally advanced pelvic cancer that requires total pelvic exenteration Expected study-specific follow-up period per patient: 5 years according to standard follow-up for this patient group Primary endpoint: R0 resection rate (circumferential resection margin \>1mm) Secondary endpoints: Rate of conversion to open surgery, peri- and postoperative complications, hospital length of stay, wound healing at 3 months follow-up, Quality of Life measured by EORTC Quality of Life Questionnaire C-30 preoperatively, at 3 months and 3 year follow-ups, disease-free survival, overall survival. Diagnosis specific endpoints. Open label observational study.

This description comes directly from the study's public registry record.

Talk to the study team

Ebbe B Thorgersen, MD PhD  ·  +4748144121  ·  ebbtho@rr-research.no

Arne M Solbakken, MD  ·  +4748281082  ·  arne.mide.solbakken@icloud.com

Always discuss trial participation with your own doctor first.

Locations (1)

Oslo University Hospital The Radium HospitalOslo, NorwayRecruiting

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Source record: clinicaltrials.gov/study/NCT05186493