Silodosin in Retrograde Intrarenal Surgery

Sponsor
Ain Shams University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05921370
Collaborator
(none)
60
1
2
4.9
12.2

Study Details

Study Description

Brief Summary

Selective alpha-blockers have been used for the treatment of ureteric stones as medical expulsive therapy (MET). Recently they have been successfully used in passive ureteric dilatation before semirigid ureteroscopy. This study enables us to know the role of silodosin in ureteric dilatation to facilitate ureteral access sheath placement in Retrograde Intrarenal Surgery with flexible ureteroscopy.

Condition or Disease Intervention/Treatment Phase
  • Drug: Silodosin 8 mg
  • Drug: Placebo
Phase 3

Detailed Description

The ureteral access sheaths (UAS) used during Retrograde Intrarenal Surgery (RIRS) were produced for easy access to the upper urinary tract. The main advantages of UAS are providing repetitive access to the ureteral and collecting duct system, decreasing intrarenal pressure, preventing bleeding-related distortion of vision by the acceleration of liquid flow, and eventually contributing toward the protection of the flexible device.

Nevertheless, there might be certain challenges during UAS placement. There are also risks, such as ureteral injury and the occurrence of ureteral stricture in the long term. However, considering the benefit/risk balance, RIRS is routinely performed in many clinics because of the ease provided by UAS.

Some problems might occur during the placement of UAS whose diameters vary between 9.5 and 14 Fr. In cases where UAS cannot be placed, manipulations can be used, such as ureteral balloon dilatation, providing access through a rigid ureteroscope with a guide wire, or dilatation with the inner sheath of the UAS, which may vary depending on the amount of personal experience. Despite such manipulations, if UAS placement is still unsuccessful, it is always more logical to place a double-J stent, enables passive dilatation, and postpone RIRS until the second operation.

This study will examine whether intramural ureteral resistance can be reduced or not and whether UAS placement can be facilitated using silodosin or not.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This prospective study will be conducted in patients prepared for RIRS presented to Ain Shams University Hospital. Group A (the study group): Patients will receive silodosin 8 mg one tablet per day for 3 days before their scheduled retrograde intrarenal surgery. Group B (the control group): Patients will receive Placebo for 3 days before their scheduled retrograde intrarenal surgery.This prospective study will be conducted in patients prepared for RIRS presented to Ain Shams University Hospital. Group A (the study group): Patients will receive silodosin 8 mg one tablet per day for 3 days before their scheduled retrograde intrarenal surgery. Group B (the control group): Patients will receive Placebo for 3 days before their scheduled retrograde intrarenal surgery.
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Effect of Perioperative Silodosin on Ureteric Dilatation in Retrograde Intrarenal Surgery
Actual Study Start Date :
Apr 4, 2023
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Silodosin group (the intervention group)

Patients will receive silodosin 8 mg one tablet per day for 3 days before their scheduled retrograde intrarenal surgery.

Drug: Silodosin 8 mg
This prospective study will be conducted on patients prepared for Retrograde intrarenal surgery presented to Ain Shams University Hospital. Patients will be randomized with 1:1 ratio into 2 equal groups. Group A (the study group): Patients will receive silodosin 8 mg one tablet per day for 3 days before their scheduled retrograde intrarenal surgery. silodosin is an alpha blocker which act to dilate the ureter to facilitate access sheath placement

Placebo Comparator: Placebo group (the control group)

Patients will receive Placebo for 3 days before their scheduled retrograde intrarenal surgery.

Drug: Placebo
This prospective study will be conducted on patients prepared for Retrograde intrarenal surgery presented to Ain Shams University Hospital. Patients will be randomized with 1:1 ratio into 2 equal groups. Group A (the study group): Patients will receive silodosin 8 mg one tablet per day for 3 days before their scheduled retrograde intrarenal surgery. Group B (the control group): Patients will receive Placebo for 3 days before their scheduled retrograde intrarenal surgery.

Outcome Measures

Primary Outcome Measures

  1. ureteric access sheath placement [intraoperative immediate diagnosis, at the beginning of surgery.]

    to assess the success of ureteric access sheath placement as follows: 1. Direct assessment: A. Success of ureteric access sheath insertion without ureteric dilatation. B. Success of ureteric access sheath insertion with ureteric dilatation. C. Failed ureteric access sheath insertion.

Secondary Outcome Measures

  1. operative time [intraoperative diagnosis during the surgery from beginning of the surgery till the end of the procedure]

    time of the procedure will be recorded from the beginning of the diagnostic cystoscopy till placement of the flexible ureteroscopy

  2. Perioperative complication [till 7 days postoperative]

    regarding of both intraoperative complications in the form of ureteric mucosal tear, ureteric avulsion, residual stones, postoperative pain, dysuria, hematuria, and fever

  3. Cost analysis [1 day post operative]

    evaluation of the cost in both arms by comparing the price for the medication for 3 days on one arm. and the cost of the supplies needed intraoperative for ureteric dilatation or the need for another surgical session

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Both sex.

  • Age >18 yrs old.

  • Upper ureteric stones or renal stones < 2 cm.

  • Patients with normal renal anatomy.

  • No history of infectious or inflammatory renal condition.

Exclusion Criteria:
  • • < 18 years old.

  • Multiple or bilateral stones.

  • Pregnant women.

  • Ureteric strictures.

  • Urinary tract infection.

  • Coagulopathy and uncorrected bleeding disorders.

  • Refusal of the surgery and requiring stent.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ahmed Maher Cairo القاهرة Egypt 11757

Sponsors and Collaborators

  • Ain Shams University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ahmed Maher Gamil Ahmed Higazy, principle investigator, Ain Shams University
ClinicalTrials.gov Identifier:
NCT05921370
Other Study ID Numbers:
  • MS 231/2023
First Posted:
Jun 27, 2023
Last Update Posted:
Jun 27, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 27, 2023