OPTIMAL STENTS DURING RENAL COLIC

Ureteral Stent Occlusion Clinical Trial

Official title: COMPARISON OF SILICONE VERSUS POLYURETHANE URETERAL STENTS: A PROSPECTIVE CONTROLLED STUDY

Status Completed

Clinical Trial Summary

From June 2018 to October 2018, patients from two distinct clinical centers were prospectively enrolled in the study and stratified (non-randomly) into either control group A, patients who received polyurethane stents (Rüsch, Teleflex), or experimental group B, patients who received silicone stents (Cook Medical). Each participant completed a survey one hour after stent insertion, in the middle of the stent dwelling period, and before stent removal or ureteroscopy noting body pain and overactive bladder via the visual analog scale pain (VASP) and overactive bladder (OAB) awareness tool, respectively. Additionally, the successfulness of stent placement, hematuria, number of unplanned visits, and stent encrustation rates were assessed within each group.

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Ureteral Stent Occlusion

• NCT number: NCT04000178
• Study type: Interventional
• Source: St. Petersburg State Pavlov Medical University
• Status: Completed
• Phase: N/A
• Start date: June 1, 2018
• Completion date: October 10, 2018