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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05833386
Other study ID # pre-FURS sildosin
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 1, 2022
Est. completion date August 1, 2026

Study information

Verified date August 2023
Source Al-Azhar University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The ureteral access sheath (UAS) is an ancillary device widely used by urologists to facilitate fast, repeatable, and safe access to ureters and collecting systems; improve visibility; reduce the risk of infection by reducing intrarenal pressure; and protect ureters and scopes when extracting multiple stones during surgery. Insertion of ureteric access sheath may be difficult due to tight ureter, so sometimes preoperative stenting might be needed. Silodosin is an α1A adrenoceptor with high affinity and selectivity for the ureteric muscle, which may reduce ureteral spasm. Oral a1-blockers can reduce intraureteral pressure, and may reduce maximal ureteral access sheath insertion force.¹ Preoperative silodosin protects against significant ureteral injury related to UAS insertion during fURS and decreases postoperative pain level. Silodosin premedication might be an effective and safe technique to replace prestenting.²


Recruitment information / eligibility

Status Recruiting
Enrollment 2000
Est. completion date August 1, 2026
Est. primary completion date May 1, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All patients with renal stones who will undergo flexible ureteroscopy and planned for using ureteral access sheath Exclusion Criteria: - Paediatric age group (less than 18 year)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Ureteral access sheath placement during flexible ureteroscope for renal stones
Ureteral access sheath placement during flexible ureteroscope

Locations

Country Name City State
Egypt Urology department - AlAzhar university Cairo

Sponsors (6)

Lead Sponsor Collaborator
Al-Azhar University Alexandria University, Benha University, Cairo University, Menoufia University, Tanta University

Country where clinical trial is conducted

Egypt, 

References & Publications (3)

Kim JK, Choi CI, Lee SH, Han JH, Shim YS, Choo MS; Young Endourological Study group. Silodosin for Prevention of Ureteral Injuries Resulting from Insertion of a Ureteral Access Sheath: A Randomized Controlled Trial. Eur Urol Focus. 2022 Mar;8(2):572-579. doi: 10.1016/j.euf.2021.03.009. Epub 2021 Mar 23. — View Citation

Koo KC, Yoon JH, Park NC, Lee HS, Ahn HK, Lee KS, Kim DK, Cho KS, Chung BH, Hong CH. The Impact of Preoperative alpha-Adrenergic Antagonists on Ureteral Access Sheath Insertion Force and the Upper Limit of Force Required to Avoid Ureteral Mucosal Injury: A Randomized Controlled Study. J Urol. 2018 Jun;199(6):1622-1630. doi: 10.1016/j.juro.2017.09.173. Epub 2018 Feb 2. — View Citation

Traxer O, Thomas A. Prospective evaluation and classification of ureteral wall injuries resulting from insertion of a ureteral access sheath during retrograde intrarenal surgery. J Urol. 2013 Feb;189(2):580-4. doi: 10.1016/j.juro.2012.08.197. Epub 2012 Oct 8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary failure rate of UAS insertion during FURS 2 hours
Secondary Ureteral injuries after UAS insertion Ureter wall injury will be classified according to the following five grades:
Grade 0: No lesion or only mucosal petechiae. Grade 1: Mucosal erosion or a mucosal flap without smooth muscle injury. Grade 2: Erosion involving the mucosa and smooth muscle but sparing the adventitia.
Grade 3: Ureteral perforation involving the full thickness of the ureteral wall, including the adventitia.
Grade 4: Total ureteral avulsion with a complete rupture of ureteral continuity.
3 hours
Secondary Post operative pain a visual analog scale (VAS) score (0 = no pain to 10 = excruciating pain) to indicate the intensity of postoperative pain 12 h after surgery. 12 hours after surgery
Secondary Complications related to the procedure will be graded using the modified Clavien-Dindo classification system. 3 months
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