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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04317443
Other study ID # 2020-01
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 1, 2020
Est. completion date September 1, 2021

Study information

Verified date April 2020
Source The International Alliance of Urolithiasis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

ESWL and PNL are the two treatment modalities for kidney stones greater than 20 mm in the pediatric population. ESWL is non-invasive, does not require anesthesia and inexpensive, but its success rate may be lower, and require multiple treatment sessions. On the contrary, PNL has a higher success rate, does not require multiple sessions but is an invasive method. Compared to standard PNL, miniaturized PNL systems have been shown to decrease complications with comparable success rates. SMP is a unique miniaturized PNL system with integrated active irrigation and suction systems. The current literature lacks studies comparing SMP and ESWL prospectively in the pediatric population. In this study, the effectiveness, reliability, and reusability of ESWL and SMP will be compared.


Description:

To compare the success and complication rates of super-mini-percutaneous nephrolithotomy (SMP) and Extracorporeal Shock Wave Lithotripsy (ESWL) for the treatment of renal stones ≥20 mm in children.An international multicentre, prospective, observational study. Pediatric cases with renal Stones ≥20 mm who undergo ESWL or SMP will be evaluated and compared proespectively. The total number of departments planned to be included in the study is 10 and the number of cases is 180.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 250
Est. completion date September 1, 2021
Est. primary completion date May 1, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 14 Years
Eligibility Inclusion Criteria:

- Children =14 years old with renal Stones =20 mm

- Willing and able to sign informed consent

- Normal renal function

- No stone-related surgical history

- American Society of Anesthesiology (ASA) score 1-2

Exclusion Criteria:

- Congenital renal anomalies (horseshoe kidney, ureteropelvic junction obstruction)

- Uncorrected UTI

- Abnormal coagulation function

- Morbid obese children (BMI=35)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Super-mini percutaneous nephrolithotomy (SMP)
SMP will be performed under general anesthesia in prone/supine position. Renal puncture will be performed under ultrasound/fluoroscopy guidance based on the preference of the participating surgeon. Tracts will be dilated to 14 Fr. Stone fragmentation will be performed with holmium laser and fragments will be extracted with the active suction system. For the exit strategy, placement of a nephrostomy tube or JJ stent will be decided by the participating surgeon.
Extracorporeal Shock Wave Lithotripsy (ESWL)
ESWL will be performed under sedation/analgesia, shock wave lithotripsy parameters will be determined based on the device and the settings of local center. For patients requiring multiple sessions, maximum 3 (or more) sessions will be allowed. Ureteral stenting prior to ESWL will be performed based on the decision of the participating center.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
The International Alliance of Urolithiasis

Outcome

Type Measure Description Time frame Safety issue
Primary Stone free rate Stone clearance on the computed tomography (2mm thickness) 3-months
Secondary blood loss Number of participants requiring blood transfusion after the procedure Postoperative day 1
Secondary auxiliary procedures Number of patients requiring additional auxiliary procedures such as second look PCNL, SWL, Ureteroscopy Postoperative month 3
Secondary hospital stay From date of admission until the date of discharge,length of hospital stay Postoperative month 3
Secondary complications Rate of postoperative complications using the Clavien-Dindo system Postoperative month 3
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