Dusting vs Basketing in RIRS: a Single-center Prospective Randomised Trial

Sponsor
Guohua Zeng (Other)
Overall Status
Unknown status
CT.gov ID
NCT03207659
Collaborator
(none)
136
1
2
16
8.5

Study Details

Study Description

Brief Summary

The investigator aims to perform a prospective and randomized controlled trial comparing the safety and efficacy of active basket extraction of fragments and stone dusting during the RIRS.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Basketing in RIRS
  • Procedure: Dusting in RIRS
N/A

Detailed Description

RIRS has been widely adopted and used by urologists worldwide in the management of renal stones due to less invasiveness and efficacy, especially in small to moderate-sized renal stones. RIRS has several advantages over SWL for stones less than 2 cm diameter. Most importantly, removing the stone in one session without the need for other treatment modalities.

Furthermore, the application of RIRS has expanded to larger stones reaching up to 35 mm in some cases,in spite of not being the first line therapy for the larger stones. RIRS has advantages over the PCNL especially concerning complications. Namely lower or no bleeding events and the less invasiveness of RIRS.

Options for the treatment of intrarenal stones include fragmenting the stone then extracting large fragments using a basket or dusting the stone into very small fragments then leaving the (dust) to pass spontaneously.

The idea of dusting in RIRS emerges as a counterpart of the originally taught fragmentation and basketing of the stones. Aiming to reduce multiple entries and exits for the renal system and ultimately not requiring UAS or baskets during the surgery. Thus theoretically decreasing operative time and costs with the same SFRs, In addition to minimizing the risk of ureteral injury .

So there is a debate amongst surgeons whether to laser the stone to dust or fragment and retrieve intra-renal fragments. EAU guidelines on the surgical management of urolithiasis stated that dusting strategies should be limited to the treatment of large renal stones. Without clearly differentiating between dusting or fragmentation and basketing. Cho et al; favored fragmentation technique especially for large renal stones because the dust in dusting technique may affect visualization and obscure small stone fragments. But this was an opinion and not built on a direct comparative study.

Until now, there is no consensus on how to achieve optimal stone clearance once the primary stone is fragmented with lithotripsy. And to date, no prospective randomized study has addressed the practice of active extraction vs. spontaneous passage

Study Design

Study Type:
Interventional
Anticipated Enrollment :
136 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Dusting vs Basketing in RIRS: a Single-center Prospective Randomised Trial
Actual Study Start Date :
Aug 1, 2017
Anticipated Primary Completion Date :
Dec 1, 2018
Anticipated Study Completion Date :
Dec 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dusting

small stones will be left to pass spontaneously.

Procedure: Dusting in RIRS
Treament of renal stones by dusting the stone under direct vision through a scope and then leaving them to pass spontaneously

Experimental: Basketing

stones will be actively extracted.

Procedure: Basketing in RIRS
Treament of renal stones by fragmentation of stone under direct vision through a flexible ureteroscope and then actively extracting them using a basket

Outcome Measures

Primary Outcome Measures

  1. Stone free rate (SFR) [4-6 weeks after surgery]

    To assess for stone-free rate using K.U.B. (kidney-ureter-bladder) plain radiograph and renal ultrasound. If there is a discrepancy in follow up imaging between the presence of residual stones or fragments between the KUB and renal ultrasound, the KUB will be considered the reference standard for small fragments less than 4mm unless the stone composition is uric acid. If fragments 5 mm or larger exist or uric acid it will be up to the discretion of the surgeon to order a CT to better delineate the presence of residual stones and their impact on the clinical management of that patient.

Secondary Outcome Measures

  1. Operating time [intraoperatively]

    from starting fragmentation to placement of stent (DJ stent or ureteral stent) unless no stent is needed

  2. Complication rates [intraoperatively or 48h postoperatively]

    Complication such as fever, pain, urosepsis etc.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients must be a suitable operative candidate for RIRS

  2. Age ≥18 years

  3. Normal renal function

  4. ASA score Ⅰ and Ⅱ

  5. Single renal stone ≤20mm or multiple stones the conglomerate diameter (additive maximal diameter of all stones on axial imaging of computed tomography) up to 20 mm

Exclusion Criteria:
  1. Pregnant subjects

  2. Uncorrected coagulopathy and active urinary tract infection (UTI)

  3. prior ipsilateral endourological procedure history, such as RIRS, PCNL, URS and URL

  4. Patients who underwent transplant or urinary diversion.

  5. Congenital abnormalities.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Urology, Minimally Invasive Surgery Center, The First Affiliated Hospital of Guangzhou Medical University Guangzhou Guangdong China 510230

Sponsors and Collaborators

  • Guohua Zeng

Investigators

  • Principal Investigator: Guohua Zeng, PH.D & MD, The First Affiliated Hospital of Guangzhou Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Guohua Zeng, Vice president, The First Affiliated Hospital of Guangzhou Medical University
ClinicalTrials.gov Identifier:
NCT03207659
Other Study ID Numbers:
  • Dusting vs Basketing in RIRS
First Posted:
Jul 5, 2017
Last Update Posted:
Aug 7, 2018
Last Verified:
Aug 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Guohua Zeng, Vice president, The First Affiliated Hospital of Guangzhou Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 7, 2018