Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03849820
Other study ID # OpeRa-2018
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date March 12, 2019
Est. completion date October 25, 2022

Study information

Verified date June 2024
Source Intuitive Surgical
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To demonstrate that Robotic-Assisted partial nephrectomy is superior to Open partial nephrectomy in reducing the number of 30 day post-operative complications (Clavien-Dindo Type I-V) for patients with intermediate to high complexity kidney tumors.


Description:

Partial nephrectomy is the surgical removal of a kidney tumor while unaffected tissue remains intact so that the kidney function is maintained as far as possible. The more radical procedure would be the complete removal of the kidney, which is not examined in this trial. Surgery will be randomized either to an open technique involving a large incision or the robotic assisted technique with a few small incisions (keyhole surgery). With robotic assisted surgery the movements of the surgeon are translated into the movement of the instruments. It is not clear which of the two procedures, open or robotic assisted, has less complications. It is expected that these are different due to the different level of invasiveness and the level of direct access to the organ. This study aims to show that robotic assisted surgery results in less complications than open surgery.


Recruitment information / eligibility

Status Terminated
Enrollment 247
Est. completion date October 25, 2022
Est. primary completion date December 15, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 years or older - Patient with a renal tumor that is a candidate for OPEN surgery and robotic assisted surgery (RAS) partial nephrectomy (PN) - R.E.N.A.L. score = 7 - eGFR = 50 ml/min/1.73 m² - Anticoagulation is accepted according to the surgeon's practice Exclusion Criteria: - Solitary kidney or functionally solitary kidney - Prior surgery at the affected kidney excluding endoscopic kidney stone surgery - Bilateral tumors - Multiple renal tumors requiring excision - Renal vein tumor thrombus - Likely insufficient volume of remaining parenchyma after partial nephrectomy to maintain viable kidney remnant - Metastatic disease with life expectancy of less than 1 year - Pregnancy or suspected pregnancy - Planned concomitant procedure - Subject who is unable or unwilling to comply with the protocol requirements - Subject considered to be from a vulnerable population according to IS0 14155:2011

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Robotic-assisted partial nephrectomy
Application of the da Vinci surgical robot to assist the partial nephrectomy
Other:
Open partial nephrectomy
Open surgery to conduct the partial nephrectomy

Locations

Country Name City State
Germany Department of Urology, University Hospital Düsseldorf Düsseldorf
Germany Department of Urology, Alfried Krupp Krankenhaus Rüttenscheid Essen
Germany Department of Urology, University Hospital Freiburg Freiburg
Germany Universitätsklinik und Poliklinik für Urologie Halle
Germany Universitätsklinikum Heidelberg, Urologische Klinik Heidelberg
Germany Klinik für Urologie, Marien Hospital Herne Herne
Germany Department of Urology - Universitätsklinikum des Saarlandes Homburg
Germany Department of Urology, University Hospital Jena Jena
Germany Klinik für Urologie, Marien-Hospital Marl Marl
Germany Department of Urology, Klinikum rechts der Isar der Technischen Universität Munich
Germany Dept. of Urology, University Hospital Tübingen Tübingen
Germany Helios Universitätsklinkum Wuppertal - Department of Urology Wuppertal

Sponsors (1)

Lead Sponsor Collaborator
Intuitive Surgical

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary 30 day complications Any complication that occurred within 30 days post surgery Day of surgery to 30th post operative day
Secondary Operative time Timing of surgical steps in the OR Day of surgery
Secondary Ischemia time Period in which the kidney has no blood supply Day of surgery
Secondary Surgical radicality conversions Conversion from robotic to open, partial to radical Day of surgery
Secondary Intraoperative blood loss Volume of blood loss during the surgical procedure Day of surgery
Secondary Pain assessment Assessment of pain level via the Brief Pain Inventory (BPI) Baseline until Day 90
Secondary Pain Medication Recording pain medication Baseline until Day 90
Secondary Neuropathic pain Development of neuropathic pain via the DN-4 Patient interview questions Baseline and Day 30 and Day 90
Secondary Kidney function via the estimated glomerular filtration rate (eGRF) Data will be gathered from routine examination, not a mandatory assessment Baseline until Day 5 / discharge (whatever is earlier)
Secondary Post operative complications Any Clavien-Dindo I-V post-operative complication Day 90
Secondary Length of stay Time from surgery to discharge Discharge
Secondary Procedure related readmissions Readmission that can be linked to the partial nephrectomy Day 90
Secondary Procedure related reoperations Re-operation that can be linked to the partial nephrectomy Day 90
Secondary Quality of recovery from the intervention Quality of recovery questionnaire QoR-9 Baseline until Day 5 / discharge (whatever is earlier)
Secondary Quality of life questionnaire, generic measure EQ-5D 5L Baseline until Day 90
Secondary Quality of life questionnaire, cancer patient specific EORTC QLQ-C30 Baseline until Day 90
Secondary Overall survival time from surgery to death from any cause Day of surgery to 5 years
Secondary Disease specific survival time from surgery to death due to kidney cancer Day of surgery to 5 years
Secondary Disease free survival time from surgery to first documented recurrence of renal cell carcinoma as defined by the investigator Day of surgery to 5 years
Secondary Local recurrence free survival Time from surgery to the first documented local recurrence e.g. tumor in the operated kidney or in the immediate vicinity (e.g. perirenal fat) at the surgical site. Portside recurrence / incisional, surgical access site recurrence to the affected kidney would also be considered as a local recurrence. Day of surgery to 5 years
Secondary Comprehensive Complication Index Any complication that occurred within 30 days post surgery Day of surgery to 30th post operative day
See also
  Status Clinical Trial Phase
Active, not recruiting NCT03634540 - A Trial of Belzutifan (PT2977, MK-6482) in Combination With Cabozantinib in Patients With Clear Cell Renal Cell Carcinoma (ccRCC) (MK-6482-003) Phase 2
Recruiting NCT03175224 - APL-101 Study of Subjects With NSCLC With c-Met EXON 14 Skip Mutations and c-Met Dysregulation Advanced Solid Tumors Phase 2
Active, not recruiting NCT00531284 - Phase 1b/2 Study of Carfilzomib in Relapsed Solid Tumors, Multiple Myeloma, or Lymphoma Phase 1/Phase 2
Recruiting NCT05842044 - NSAID Use After Robotic Partial Nephrectomy Phase 2
Recruiting NCT05387863 - Decision Aid (DA) for Renal Patients N/A
Terminated NCT02669914 - MEDI4736 (Durvalumab) in Patients With Brain Metastasis From Epithelial-derived Tumors Phase 2
Completed NCT04933604 - LPN in Patients With High-complex Renal Tumors
Withdrawn NCT03390413 - Robot-assisted Surgical Resection vs. Cryoablation of Localised Renal Cancer N/A
Recruiting NCT05119335 - A Study of NKT2152, a HIF2α Inhibitor, in Patients With Advanced Clear Cell Renal Cell Carcinoma Phase 1/Phase 2
Active, not recruiting NCT03203473 - Study of Optimized Management of Nivolumab Based on Response in Patients With Advanced RCC (OMNIVORE Study) Phase 2
Suspended NCT04115254 - Stereotactic Magnetic Resonance Guided Radiation Therapy N/A
Enrolling by invitation NCT02609269 - Decipher Genomics Resource for Intelligent Discovery
Terminated NCT01453595 - BEZ235 in Patients With Advanced Renal Cell Carcinoma (RCC) Phase 1/Phase 2
Completed NCT01444456 - Assessment of Quality of Life in Patients With Symptomatic Chemotherapy-induced Anaemia N/A
Completed NCT02811250 - Stereotactic Radiotherapy for Renal Cancers N/A
Completed NCT00398814 - Phase I Study of Perifosine + Sorafenib for Patients With Advanced Cancers Phase 1
Completed NCT00399152 - Perifosine + Sunitinib Malate for Patients With Advanced Cancers Phase 1
Completed NCT00458536 - Vaccination of Patients With Renal Cell Cancer With Dendritic Cell Tumor Fusions and GM-CSF Phase 1/Phase 2
Recruiting NCT03693014 - A Study of Several Radiation Doses for Patients With Progression on Immunotherapy/Checkpoint Inhibitors Phase 2
Completed NCT00418496 - Interleukin-2 With Sorafenib (BAY 43-9006) for Unresectable or Metastatic Clear Cell Renal Carcinoma (RCC) and Metastatic Melanoma Phase 1