Safety and Efficacy of Fluoroscopy-free Technique During Retrograde Intrarenal Surgery for Renal Stones
Primary Purpose
Kidney Calculi, Radiation Exposure, Retrograde Intrarenal Surgery
Status
Recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Fluoroscopy-free RIRS
Standard RIRS
Sponsored by
About this trial
This is an interventional treatment trial for Kidney Calculi
Eligibility Criteria
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.
Sites / Locations
- Urology Department, Al-Azhar University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Fluoroscopy-free RIRS
Standard RIRS
Arm Description
Patients will be treated by RIRS without fluoroscopy
Standard RIRS under fluoroscopy-guidance will be performed
Outcomes
Primary Outcome Measures
stone-free rate
defined as no residual stone or residual fragment(s) less than 4 mm (as confirmed by CT-UT).
complication rate
intraoperative and postoperative complications
Secondary Outcome Measures
fluoroscopy time
intraoperative fluoroscopy imaging
Operative time
Time from induction of anesthesia till the end of the procedure
the need for fluoroscopy
The need for fluoroscopy imaging in a fluoroscopy-free group
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05269108
Brief Title
Safety and Efficacy of Fluoroscopy-free Technique During Retrograde Intrarenal Surgery for Renal Stones
Official Title
Safety and Efficacy of Fluoroscopy-free Technique During Retrograde Intrarenal Surgery for Renal Stones: A Prospective, Randomized, Non-inferiority Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 25, 2022 (Actual)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
April 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Al-Azhar University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. 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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Calculi, Radiation Exposure, Retrograde Intrarenal Surgery
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The 1st group: Fluoroscopy-free RIRS. The 2nd group: Fluoroscopy-guided RIRS.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
520 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Fluoroscopy-free RIRS
Arm Type
Experimental
Arm Description
Patients will be treated by RIRS without fluoroscopy
Arm Title
Standard RIRS
Arm Type
Active Comparator
Arm Description
Standard RIRS under fluoroscopy-guidance will be performed
Intervention Type
Procedure
Intervention Name(s)
Fluoroscopy-free RIRS
Intervention Description
RIRS for renal stone under direct visualization, without fluoroscopy
Intervention Type
Procedure
Intervention Name(s)
Standard RIRS
Intervention Description
RIRS for renal stone under fluoroscopy-guidance
Primary Outcome Measure Information:
Title
stone-free rate
Description
defined as no residual stone or residual fragment(s) less than 4 mm (as confirmed by CT-UT).
Time Frame
3-months after the intervention.
Title
complication rate
Description
intraoperative and postoperative complications
Time Frame
intraoperative till 3-months postoperative complications
Secondary Outcome Measure Information:
Title
fluoroscopy time
Description
intraoperative fluoroscopy imaging
Time Frame
intraoperative
Title
Operative time
Description
Time from induction of anesthesia till the end of the procedure
Time Frame
The procedure time
Title
the need for fluoroscopy
Description
The need for fluoroscopy imaging in a fluoroscopy-free group
Time Frame
Intraoperative
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Abul-fotouh Ahmed, MD
Phone
00201001066756
Email
abulfotouhahmed@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abul-fotouh Ahmed, MD
Organizational Affiliation
Al-Azhar University Hospitals, Cairo, Egypt
Official's Role
Principal Investigator
Facility Information:
Facility Name
Urology Department, Al-Azhar University Hospital
City
Cairo
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ahmed Fahim, MD
Phone
002025107333
Email
urologyhospital@gmail.com
First Name & Middle Initial & Last Name & Degree
Ahmed El-Garhi, MD
12. IPD Sharing Statement
Learn more about this trial
Safety and Efficacy of Fluoroscopy-free Technique During Retrograde Intrarenal Surgery for Renal Stones
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