In vitro evaluation of an innovative biocompatible Adhesive for complete retrieval of residual fragments after lithotripsy

• Conditions: urinary calculus; N20-N23; Urolithiasis

• Registration Number: DRKS00010243
• Lead Sponsor: niversitätsklinikum FreiburgDepartment ChirurgieKlilnik für Urologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-03-31
• Study Completion: 2016-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 15

Inclusion Criteria

inclusion of human stone probes of patients with conventional treatment. Stone probes would be disposed. No patients are included into the present study.

Exclusion Criteria

Patients/stone probes of patients < 18 years

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
endoscopic and macroscopic stone-free rate

Secondary Outcome Measures

Name	Time	Method
time to complete stone clearance, extraction efficancy