Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02807376 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by Ethicon Endo-Surgery.

Completed
Registry status
NA
Development phase
270
Enrollment target

NCT02807376: Completed NA study, sponsored by Ethicon Endo-Surgery.

NCT02807376 is a NA study that has completed, run by Ethicon Endo-Surgery. The registered enrollment target is 270 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02807376, a NA study, has completed, sponsored by Ethicon Endo-Surgery.

COMPLETED
Registry status
NA
Development phase
270 participants
Enrollment target

Study 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

Primary Outcome

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 i

Interventions

  • DEVICE Surgeon's 'standard of care' stapler
  • DEVICE Ethicon Powered Vascular Stapler

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2016-07-05
Est. Completion 2017-08-23
Phase NA
Ethicon Endo-Surgery

39 total trials

What the finished NCT02807376 record still lists

NCT02807376 is an interventional study that assigns participants to a tested intervention. The registered 270 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 2 interventions - of which Surgeon's 'standard of care' stapler is the first listed.

NCT02807376 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02807376 about?

NCT02807376 is a clinical study titled "An Evaluation of a Powered Vascular Stapler in Laparoscopic Nephrectomies and Nephroureterectomies". 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

What is the current status of trial NCT02807376?

This trial is currently completed. It is a NA study. The enrollment target is 270 participants. The study started on 2016-07-05. Estimated completion is 2017-08-23.

What interventions are being tested in trial NCT02807376?

The interventions under investigation include: Surgeon's 'standard of care' stapler (DEVICE), Ethicon Powered Vascular Stapler (DEVICE).

Who is sponsoring clinical trial NCT02807376?

This trial is sponsored by Ethicon Endo-Surgery, which has 39 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02807376's enrollment target sits among peer trials

270 387th of 2000 higher than 1,609 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00801489 · 270 participants · Phase 2

    Fludarabine Phosphate, Cytarabine, Filgrastim-sndz, Gemtuzumab Ozogamicin, and Idarubicin Hydrochloride in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome

  • NCT04372485 · 270 participants · NA

    Using Mobile Health (mHealth) to Improve STI Treatment Adherence Among Adolescents

  • NCT04528446 · 270 participants

    The Impact of Glomerular Disorders on Bone Quality and Strength

  • NCT05215327 · 270 participants · Phase 2

    High vs. Standard Dose Influenza Vaccine in Lung Allograft Recipients

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02807376, the US trial registry maintained by the National Library of Medicine. NCT02807376 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.