Clinical Trials Directory

Trials / Completed

CompletedNCT03087812

Durability of Flexible Ureteroscopes and Causes of Infection During Flexible Ureterorenoscopy

Status
Completed
Phase
Study type
Observational
Enrollment
400 (actual)
Sponsor
Clinical Research Office of the Endourological Society · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is an observational study in which data on consecutive patients who undergo ureterorenoscopy with the use of a flexible ureterorenoscope are collected. In total 20 new ureteroscopes are usedfrom Olympus andfrom Storz) to study the durability of the ureteroscopes and the possible microbiological load.

Detailed description

This is an observational study in which data on consecutive patients who undergo ureterorenoscopy with the use of a flexible ureterorenoscope are collected. In total 6 new ureteroscopes are used (3 from Olympus and 3 from Storz) to study the durability of the ureteroscopes and the possible microbiological load. Before the procedure is started the endoscope is tested for its microbiological load in two different ways:1. Shake the tip of the flexible ureterorenoscope 5 seconds in a sterile container filled with 10 cc of NaCl 0.9% 2. Flush the working channel of the ureterorenoscope with 10 cc of NaCl 0.9% and collect the sample in a sterile container. After the procedure is finished, the endoscope is tested for its microbiological load in two different ways: 1\. Shake the tip of the flexible ureterorenoscope 5 seconds in a sterile container filled with 10 cc of NaCl 0.9% 2. Flush the working channel of the ureterorenoscope with 10 cc of NaCl 0.9% and collect the sample in a sterile container. Transfer all samples to the lab as soon as possible but at least within four hours after collecting the samples. As for the clinical efficacy during each procedure a detailed questionnaire about the use of each ureteroscope is filled out. This includes the ease of use making mention on quality of the image, torque, flexibility and durability. Data will be collected through electronic case report forms (eCFRs), with use of an online Data Management system (DMS).

Conditions

Timeline

Start date
2015-12-01
Primary completion
2017-12-01
Completion
2017-12-01
First posted
2017-03-23
Last updated
2018-04-10

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT03087812. Inclusion in this directory is not an endorsement.