Viewing Study NCT04731090



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Last Modification Date: 2024-10-26 @ 1:55 PM
Study NCT ID: NCT04731090
Status: COMPLETED
Last Update Posted: 2021-01-29
First Post: 2021-01-25

Brief Title: Standard Antibiotic Versus Enhanced Prophylactic Measures on Rate of Urinary Tract Infection After Flexible Ureteroscopy
Sponsor: Egyptian Biomedical Research Network
Organization: Egyptian Biomedical Research Network

Study Overview

Official Title: Effect of Standard Antibiotic Prophylaxis Versus Enhanced Prophylactic Measures on Rate of Urinary Tract Infection After Flexible Ureteroscopy
Status: COMPLETED
Status Verified Date: 2021-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Background and aim Urinary tract infections UTIs are commonly seen after flexible ureteroscopy Prevention of UTIs remains controversial The present randomized study aimed to compare the rate of post-procedural UTI in patients subjected to the standard antibiotic prophylaxis alone versus enhanced prophylactic measures

Patients and methods The study included 100 patients subjected to fURS for management of ureteral andor renal stones Patients were equally and randomly allocated into one of the two treatment groups using randomly computer-generated allocation tables and concealed envelope technique Treatment groups included standard antibiotic prophylaxis group and enhanced prophylaxis group Patients in the standard antibiotic prophylaxis group IV fluoroquinolone 1 hour preoperatively and oral antibiotics were used for 24h postoperatively In the enhanced prophylaxis group patients had urine culture 10 days before the procedure In addition to the antibiotic prophylaxis hydrophilic-coated ureteral access sheaths were systematically used
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None