Viewing Study NCT06465784



Ignite Creation Date: 2024-07-17 @ 11:03 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06465784
Status: COMPLETED
Last Update Posted: 2024-06-20
First Post: 2024-05-29

Brief Title: Laser Lithotripsy for Ureteral Stones
Sponsor: Mahmoud Helmy El saeed Hussein
Organization: Al-Azhar University

Study Overview

Official Title: Comparison Between Retrograde and Antegrade Ureteroscopic Laser Lithotripsy for Management of Medium Sized Proximal Ureteral Stones A Randomized Prospective Study
Status: COMPLETED
Status Verified Date: 2024-06
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: Objectives To present the outcomes of retrograde and antegrade ureteroscopic laser lithotripsy in the treatment of proximal ureteral stones ranging in size from 10 to 20 millimeters in diameter

Patients and methods From March 2023 to December 2023 70 patients were included in this prospective randomized double-arm interventional study Patients were divided into two groups Group 1 35 patients had semi-rigid retrograde ureteroscopic laser lithotripsy and group 2 35 patients had semi-rigid antegrade ureteroscopic laser lithotripsy
Detailed Description: The present study was conducted in Al-Azhar University Hospital Damietta branch urology departmentat the period from March 2023 to December 2023 Seventy patients with symptomatic proximal medium sized ureteric stones were classified in two groups Retrograde Uretroscopic Laser Lithotripsy group 1 and Antegrade Ureteroscopic Laser Lithotripsy group 2

The preoperative-patient- and stone-related intraoperative- and postoperative- related parameters that might influence the perioperative course and short-term clinical outcomes were evaluated

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