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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02645058
Other study ID # 0016589
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2, 2015
Est. completion date June 19, 2019

Study information

Verified date May 2020
Source University of Turin, Italy
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the effectiveness of RIRS (retrograde intrarenal surgery) and ESWL (extracorporeal shockwaves lithotripsy) in the treatment of renal stone ranging form 6 to 20 mm size.


Description:

European urological guidelines consider RIRS and ESWL the treatments of choice for renal stones < 20 mm. RIRS is a endoscopic surgery which allows to rich the kidney from the ureter. A flexible ureteroscope is used for these kind of procedure. Through this device a laser fiber (Holmium laser) is used to treat the stones. After that, small fragments can be removed with a basket. In some cases, according to intraoperative findings, a ureteral stent can be push in the kidney to help the drainage of the kidney. ESWL is a procedure which allows to treat the stones by shock waves generated by a specific machine which work in direct contact with the skin of the patients (extracorporeal). Shockwaves pass all the tissues and finally reach the stones. Such energy allows to break the stones in small fragments, that wll be spontaneously passed by the patients. Specific parameters of these treatments are discussed in "Arms and Interventions". Many studies demonstrated high success rate of RIRS and this technique is becoming more and more adopt. One study demonstrated better outcomes of RIRS versus ESWL, but only for renal stones located in the inferior calices and smaller then 10 mm. There are not other studies comparing the two procedures and there are not proofs that RIRS ensures better outcomes for other renal stones (neither for size nor for location).


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date June 19, 2019
Est. primary completion date May 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- renal stone measuring 6 to 20 mm

- signing informed consent

- WHO performance status 0-2

Exclusion Criteria:

- Other stone >5 mm

- concomitant ureteral stones

- BMI > 35

- severe coagulopathy

- impossibility to sign informed consent

- pregnancy

- age < 18 years old or > 85

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
RIRS
Treatment by ureterorenoscopy (RIRS) and laser lithotripsy
ESWL
Treatment by extracorporeal shock waves lithotripsy
Device:
Rigid and flexible ureteroscope

Lithotripter

Holmium laser

Basket for fragment removal

Procedure:
General or spinal anesthesia

Drug:
Intravenous pain medication
If required by the patient
Device:
X-ray
To focus the stone
Ultrasound
To focus the stone

Locations

Country Name City State
Italy Urology, University of Turin Turin

Sponsors (1)

Lead Sponsor Collaborator
University of Turin, Italy

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients stone free SFR 4 Patients with residual fragments < 5 mm after treatment 1 month from treatment
Secondary Number of patients stone free SFR 0 Patients with no residual fragments after treatment 1 month from treatment
Secondary Number of patients stone free SFR 4 Patients with residual fragments < 5 mm after treatment 6 months after the treatment
Secondary Number of patients stone free SFR 0 Patients with no residual fragments after treatment 6 months after the treatment
Secondary Number of patients stone free SFR 4 Patients with residual fragments < 5 mm after treatment 1 year after the treatment
Secondary Number of patients stone free SFR 0 Patients with no residual fragments after treatment 1 year after the treatment
Secondary rate of complications number of complications after treatment within 1 month form treatment
Secondary rate of further treatment needed number of retreatment within 1 year
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