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Clinical Evaluation of BackStop in Patients Undergoing Ureteroscopic Lithotripsy

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University of Southern California

Status

Terminated

Conditions

Kidney Stones

Treatments

Device: BackStop

Study type

Interventional

Funder types

Other

Identifiers

NCT02122341
HS-12-00714

Details and patient eligibility

About

The purpose of this clinical study is to evaluate BackStop, a polymer-based device that is intended to be used during ureteroscopic lithotripsy to prevent retrograde stone migration.

Full description

During ureteroscopic treatment for ureteral stones, lithotripsy, irrigation, and manipulation of the stone often pushes stone away into the kidney itself. This phenomenon is called retropulsion, which is defined as clinically significant retrograde migration of stone or stone fragments. Movement of stones retrograde into the renal pelvis could potentially add and complicate the surgery further. Often scopes need to be changed in order to reach the stone, and chasing these stones will add time to the surgery and require more valuable resources. Furthermore, sometimes a second operation will need to be done when these retropulsed fragments could not be all found and cleaned out.

A number of devices have been developed to prevent such migration including stone baskets and conical devices. These are wire-based devices which have the potential of injuring the ureter. Because of safety concerns and that there is limited data available on the effectiveness of these devices; these are not widely used by urologists. BackStop has recently been developed as another tool to prevent retropulsion. It is a water soluble gel that is injected proximal to the stone. This creates a physical barrier that prevents stone migration during ureteroscopic lithotripsy for ureteral calculus.

Enrollment

35 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patient with solitary ureteral stone ranging from 5mm to 15mm diameter
  • able to tolerate general anesthesia
  • clinical indication for treatment by ureteroscopic lithotripsy
  • must be willing and able to participate in any follow-up visits
  • provide informed consent
  • have a CT scan demonstrating the stone

Exclusion criteria

  • patients undergoing extracorporeal shock wave lithotripsy (ESWL) or any other extracorporeal or percutaneous lithotripsy procedure as primary procedure
  • any co-morbidity or condition that would necessitate exclusion of patient (physician opinion)
  • renal or ureteral anatomical abnormality
  • multiple stones in the indicated ureter
  • stones in the indicated kidney
  • patient is immunocompromised
  • multiple organ dysfunction syndrome
  • has an absolute or relative solitary kidney mass
  • >= Stage 3 chronic kidney disease
  • bilateral ureteral obstructing stones
  • staghorn calculi
  • impaction of several stone fragments (Steinstrasse)
  • uncorrected coagulopathy/thrombocytopenia
  • urethral and/or ureteral stricture
  • reconstructive urinary surgery

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

35 participants in 2 patient groups

BackStop
Experimental group
Description:
Patients randomized to the Experimental arm will receive the BackStop gel during their ureteroscopic lithotripsy to prevent retrograde migration of stones or stone fragments.
Treatment:
Device: BackStop
Control
No Intervention group
Description:
Patients randomized to the control group will not use any devices to prevent retrograde migration of stones and stone fragments during their ureteroscopic lithotripsy.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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