Skip to main content
Clinical Trials/NCT04534998
NCT04534998UnknownPhase 2

ROBOtic-assisted Versus Conventional Open Partial Nephrectomy: a Single-center, Open-label, Randomized Controlled Feasibility Trial

Universitätsmedizin Mannheim1 site in 1 country50 target enrollmentStarted: June 15, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 2
Enrollment
50
Locations
1
Primary Endpoint
Recruitment rate

Study Overview

Brief Summary

ROBOCOP is an open-label, randomized controlled feasibility trial comparing robotic-assisted and open partial nephrectomy in preparation for a confirmative phase III randomized controlled trial.

Detailed Description

Surgical excision is the gold standard for the treatment for localized kidney cancer. An organ-preserving procedure should be carried out whenever possible in order to maintain kidney function. Partial nephrectomy can be performed through the conventional open technique as well as through a robotic-assisted approach. Although both methods belong to the standard care, there is still no published data from randomized controlled trials in the scientific literature comparing them. The ROBOCOP-trial is designed as a single-center comparison of the two surgical approaches in preparation for a phase III study. 50 patients are to be included in the trial within a period of 15 months. The primary endpoint is feasibility of patient recruitment. In addition, potential primary outcomes for a confirmative trial such as perioperative complications, quality of life, inflammatory response, survival and ergonomic aspects for the operating surgeons will be investigated.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •scheduled for elective partial nephrectomy for renal neoplasms
  • •Patient must be at least 18 years old and capable to consent
  • •abdominal MRI or CT scan
  • •curative-intent surgery
  • •robotic-assisted and open approach for surgery are both feasible
  • •ability of patient to understand the goal, consequences and alternatives of participation in the trial
  • •written informed consent

Exclusion Criteria

  • •patients with solitary kidney
  • •multiple kidney tumors
  • •emergency intervention, for example because of bleeding or perforation
  • •2nd malignancy that will make PN needless, this does not include secondary malignancies which are under curative treatment or cases in which death from RCC is more likely
  • •patient belongs to a vulnerable patient group
  • •simultaneous 2nd surgery

Arms & Interventions

Robotic-assisted partial nephrectomy

Experimental

Partial nephrectomy will be performed using a robotic-assisted laparoscopic approach.

Intervention: Partial nephrectomy (Procedure)

Open partial nephrectomy

Active Comparator

Partial nephrectomy will be performed using an open retroperitoneal approach.

Intervention: Partial nephrectomy (Procedure)

Outcomes

Primary Outcomes

Recruitment rate

Time Frame: 15 months

Proportion of randomized patients in relation to the eligible ones.

Secondary Outcomes

  • Inflammatory response(throughout patient´s hospital stay, on average 6 days)
  • Perioperative complications(throughout patient´s hospital stay, on average 6 days)
  • Length of hospital stay(throughout patient´s hospital stay, on average 6 days)
  • Postoperative self-reported quality of life(90 days)
  • Conversion to radical nephrectomy(Immediately after surgery)
  • Case cost(90 days)
  • Self-reported quality of life in patients with kidney disease(90 days)
  • Resection status(up to 5 days)
  • Use of analgesia(throughout patient´s hospital stay, on average 6 days)
  • Blood loss(Immediately after surgery)
  • Conversion to open surgery(Immediately after surgery)
  • Kidney function - creatinine(90 days)
  • Trifecta outcomes of partial nephrectomy(90 days)
  • Postoperative complications(90 days)
  • Kidney function - GFR(90 days)
  • Self-reported generic health status(90 days)
  • Self-reported quality of life assessment of cancer patients(90 days)
  • Self-assessment of depression in patients ≥ 65 years old(90 days)
  • Self-evaluation of cancer disease´s influence on elderly patients´ life(90 days)
  • Self-assessment of comorbidity in elderly patients(90 days)
  • Operative time(Immediately after surgery)
  • Inflammatory response - leucocytes(throughout patient´s hospital stay, on average 6 days)
  • Inflammatory response - C-reactive protein(throughout patient´s hospital stay, on average 6 days)
  • Surgical ergonomics(During surgery)
  • Surgical ergonomics(Immediately after surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Karl-Friedrich Kowalewski

Principal Investigator

Universitätsmedizin Mannheim

Study Sites (1)

Loading locations...

Similar Trials