Safety and Efficacy of Fluoroscopy-free Technique During Retrograde Intrarenal Surgery for Renal Stones

Sponsor
Al-Azhar University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05269108
Collaborator
(none)
400
1
2
25.2
15.9

Study Details

Study Description

Brief Summary

Aiming to reduce radiation exposure to patients and physicians, the investigators conduct this study protocol to evaluate the possibility of performing retrograde intrarenal surgery (RIRS) under direct visualization without fluoroscopy. the investigators will prospectively evaluate the outcome of fluoroscopy-free RIRS for renal stones in comparison with the standard technique. The investigators expected that the fluoroscopy-free technique has high safety and efficacy even in complicated cases.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Fluoroscopy-free RIRS
  • Procedure: Standard RIRS
N/A

Detailed Description

With improved flexible URS instrumentation and lithotripsy technology, retrograde intrarenal surgery (RIRS) became an alternative and excellent option for renal stones. Fluoroscopy imaging may be necessary during various steps of RIRS, such as insertion of a guidewire and stent, access sheath insertion, detection of stone location and size, and assessment of collecting system anatomy.

In an effort to decrease radiation exposure, several studies were conducted to evaluate the possibility of performing RIRS under direct visualization without fluoroscopy. Most studies concluded that fluoroscopy-free RIRS is a feasible, effective, and safe technique. The reported stone-free rate ranged from 83.8% to 95.7%. No major complications were observed.

Despite the reported high safety and efficacy of the fluoroscopy-free RIRS technique, most of the studies were retrospective and included only uncomplicated cases, and none of the studies address its results against control.

In the present study, the investigators will prospectively evaluate the efficacy and safety of fluoroscopy-free RIRS for renal stones in comparison with fluoroscopy-guided technique as standard control. The study will include all patients with renal stones amenable to RIRS. The investigators expected that the fluoroscopy-free technique can deal with large stones and complex situations with high safety and success rate. The study hypothesis is that "the fluoroscopy-free technique has efficacy and safety similar to the fluoroscopy-guided technique".

The investigators also aim to determine the patients and surgical characteristics impacting the need for fluoroscopy. The intra-operative fluoroscopy imaging is expected to be necessary during RIRS, especially in complicated cases. In the fluoroscopic-free group, the fluoroscopic equipment will be available in the operating room and will be used if needed.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The 1st group: Fluoroscopy-free RIRS. The 2nd group: Fluoroscopy-guided RIRS.The 1st group: Fluoroscopy-free RIRS. The 2nd group: Fluoroscopy-guided RIRS.
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Safety and Efficacy of Fluoroscopy-free Technique During Retrograde Intrarenal Surgery for Renal Stones: A Prospective, Randomized, Non-inferiority Trial
Actual Study Start Date :
Feb 25, 2022
Anticipated Primary Completion Date :
Feb 1, 2024
Anticipated Study Completion Date :
Apr 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Fluoroscopy-free RIRS

Patients will be treated by RIRS without fluoroscopy

Procedure: Fluoroscopy-free RIRS
RIRS for renal stone under direct visualization, without fluoroscopy

Active Comparator: Standard RIRS

Standard RIRS under fluoroscopy-guidance will be performed

Procedure: Standard RIRS
RIRS for renal stone under fluoroscopy-guidance

Outcome Measures

Primary Outcome Measures

  1. stone-free rate [3-months after the intervention.]

    defined as no residual stone or residual fragment(s) less than 4 mm (as confirmed by CT-UT).

  2. complication rate [intraoperative till 3-months postoperative complications]

    intraoperative and postoperative complications

Secondary Outcome Measures

  1. fluoroscopy time [intraoperative]

    intraoperative fluoroscopy imaging

  2. Operative time [The procedure time]

    Time from induction of anesthesia till the end of the procedure

  3. the need for fluoroscopy [Intraoperative]

    The need for fluoroscopy imaging in a fluoroscopy-free group

Eligibility Criteria

Criteria

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

  • Stone size: ≥10 mm.

Exclusion Criteria:
  • Partial and complete staghorn stones.

  • Pregnant women.

  • Morbid obesity.

  • Uncorrectable coagulation disorders.

  • Active urinary tract infection (UTI).

  • Stone in a calyceal diverticulum.

  • Urinary tract obstruction distal to the stone.

  • Concomitant pathology that needs intervention in the same setting.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Urology Department, Al-Azhar University Hospital Cairo Egypt

Sponsors and Collaborators

  • Al-Azhar University

Investigators

  • Principal Investigator: Abul-fotouh Ahmed, MD, Al-Azhar University Hospitals, Cairo, Egypt

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Abul-fotouh Ahmed, Professor, Al-Azhar University
ClinicalTrials.gov Identifier:
NCT05269108
Other Study ID Numbers:
  • Uro_Azhar_2_022
First Posted:
Mar 7, 2022
Last Update Posted:
Mar 7, 2022
Last Verified:
Feb 1, 2022
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 Mar 7, 2022