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An Evaluation of a Powered Vascular Stapler in Laparoscopic Nephrectomies and Nephroureterectomies

Not Applicable
Completed
Conditions
Excision of Kidney
Interventions
Device: Ethicon Powered Vascular Stapler
Device: Surgeon's 'standard of care' stapler
Registration Number
NCT02807376
Lead Sponsor
Ethicon Endo-Surgery
Brief Summary

This prospective, randomized, controlled, multi-center study will collect and compare data from the surgeon's current standard of care stapler (for renal artery and renal vein transection) and powered vascular stapler

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
270
Inclusion Criteria
  • Scheduled for a simple or radical laparoscopic nephrectomy or a laparoscopic nephroureterectomy in accordance with the institution's standard of care (SOC);
  • Performance status 0-1 (Eastern Cooperative Oncology Group classification), if applicable;
  • American Society of Anesthesiologists (ASA) score < 3;
  • No prior history of partial or wedge nephrectomy (on the kidney in which the procedure will be performed);
  • Willing to give consent and comply with study-related evaluation and treatment schedule; and
  • At least 18 years of age
Exclusion Criteria
  • Prior chemotherapy or radiation (within 30 days prior to the procedure or the duration of the subject's enrollment);
  • Pregnancy;
  • Physical or psychological condition which would impair study participation; or
  • The subject is judged unsuitable for study participation by the Investigator for any other reason.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Ethicon Powered Vascular StaplerEthicon Powered Vascular StaplerEthicon Powered Vascular Stapler
Surgeon's 'standard of care' staplerSurgeon's 'standard of care' staplerSurgeon's standard of care stapler
Primary Outcome Measures
NameTimeMethod
Proportion of Vessels Transected Requiring Intra-Operative Hemostatic InterventionsIntra-Operative, an average of 2.6 hours, ranging from 42 minutes to 6.4 hours

Proportion of hemostatic interventions/procedures completed for intra-operative bleeding related to the transection of the Reanl Artery and Renal Vein during laparoscopic nephrectomy or nephroureterectomy with the use of standard of care stapler (SOC) or powered vascular stapler (PVS) defined as bleeding detected and controlled intraoperatively (additional stapling, over-sewing, clip placement, compression, use of suture, sealant, and/or buttress, and/or use of energy); or bleeding that occurs intra-operatively requiring blood or blood product transfusion or an additional surgical procedure (e.g. conversion to open).

Secondary Outcome Measures
NameTimeMethod
Proportion of Participants Requiring Post-operative Interventions or Procedures Related to Renal Artery or Renal Vein BleedingPost-Op through 4 Week Follow-up

Proportion of participants with hemostatic interventions /procedures completed for post-operative bleeding related to the transection of the Renal Artery and Renal Vein during laparoscopic nephrectomy or nephroureterectomy with the use of SOC or PVS:

* Hemostasis intervention: bleeding that occurs post-operatively requiring blood or blood product transfusion or an additional surgical procedure (related to Renal Artery and Renal Vein transection).

No hemostasis intervention is defined as no interventions needed for post-operative bleeding (related to PA and PV transection).

Trial Locations

Locations (1)

Emory University

🇺🇸

Atlanta, Georgia, United States

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