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Effect of Preop Stent Duration on SFR and Secondary Intervention in RIRS

Evaluation of the Effect of Preoperative Stenting Duration on Stone-Free Rates and the Need for Secondary Surgical Intervention in Retrograde Intrarenal Surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07052188
Enrollment
210
Registered
2025-07-04
Start date
2025-06-26
Completion date
2026-03-28
Last updated
2026-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stone, Kidney, Stone, Urinary

Keywords

Ureteral stent, retrograde intrarenal surgery, prestenting, preoperative ureteral stenting

Brief summary

This study aims to evaluate how placing a stent before surgery (preoperative stenting or passive dilation) affects the success rate of retrograde intrarenal surgery (RIRS), which is performed for kidney stones. Specifically, we will examine whether stenting improves the chance of becoming stone-free after surgery and reduces the need for a second surgical procedure.

Interventions

PROCEDUREwithout any preoperative stenting

Patients will have RIRS without any preoperative stenting.

PROCEDURE(DJ) stent placed with sedation and undergo RIRS within 2-4 weeks

Patients will have a double-J (DJ) stent placed with sedation and undergo RIRS within 2-4 weeks.

PROCEDUREPatients will have a DJ stent placed with sedation and undergo RIRS within 4-6 weeks.

Patients will have a DJ stent placed with sedation and undergo RIRS within 4-6 weeks

Sponsors

Bedreddin Kalyenci
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients over 18 years of age with an indication for RIRS (Retrograde Intrarenal Surgery)

Exclusion criteria

* Patients under 18 or over 65 years of age * Patients who cannot be followed up in the postoperative period

Design outcomes

Primary

MeasureTime frame
Number of Participants with stone-freein the first month after surgery
Number of Participants with additional surgery was neededin the first month after surgery

Secondary

MeasureTime frame
Number of Participants with postoperative complicationswithin 1 month after surgery

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 14, 2026