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Recruiting NCT07535281

NCT07535281 Effect of Complete Suction-Induced Collapse of the Renal Collecting System at the End of RIRS on Early Postoperative Outcomes

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Clinical Trial Summary
NCT ID NCT07535281
Status Recruiting
Phase
Sponsor Kangdong Sacred Heart Hospital
Condition Kidney Stones
Study Type INTERVENTIONAL
Enrollment 90 participants
Start Date 2026-04-20
Primary Completion 2027-09

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Complete suction-induced collapseStandard RIRS with natural drainage

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 90 participants in total. It began in 2026-04-20 with a primary completion date of 2027-09.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to evaluate whether actively suctioning the renal collecting system to induce a "collapse" state at the end of retrograde intrarenal surgery (RIRS) can reduce postoperative pain and infection in patients with kidney stones. Participants will be randomly assigned to either the experimental group (suction-induced collapse) or the control group (standard drainage). The study aims to determine if this simple surgical modification can improve early recovery outcomes and patient satisfaction.

Eligibility Criteria

Inclusion Criteria: * Patients aged 20 to 80 years. * Patients diagnosed with kidney stones and scheduled for retrograde intrarenal surgery (RIRS). * Patients who have voluntarily signed the written informed consent form Exclusion Criteria: * Participation in another clinical trial (drug or device) within 1 month prior to enrollment. * Congenital abnormalities of the urinary or reproductive system. * Presence of a pre-placed ureteral stent (pre-stenting) at the time of surgery. * Solitary kidney. * Uncontrolled urinary tract infection. * History of ureteral reconstruction on the affected side. * Pregnancy. * Uncorrectable bleeding diathesis or ongoing therapeutic anticoagulation therapy. * Contraindications to general anesthesia. * Other conditions that the investigator deems inappropriate for participation in the study.

Contact & Investigator

Central Contact

Han Kyu Chae, M.D., Ph.D.

✉ hanqsinopoli@gmail.com

📞 +821091869125

Principal Investigator

Han Kyu Chae, M.D., Ph.D.

PRINCIPAL INVESTIGATOR

Department of Urology, Kangdong Sacred Heart Hospital, Hallym University College of Medicine

Frequently Asked Questions

Who can join the NCT07535281 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, up to 80 Years, studying Kidney Stones. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07535281 currently recruiting?

Yes, NCT07535281 is actively recruiting participants. Contact the research team at hanqsinopoli@gmail.com for enrollment information.

Where is the NCT07535281 trial being conducted?

This trial is being conducted at Gandong-gu, South Korea.

Who is sponsoring the NCT07535281 clinical trial?

NCT07535281 is sponsored by Kangdong Sacred Heart Hospital. The principal investigator is Han Kyu Chae, M.D., Ph.D. at Department of Urology, Kangdong Sacred Heart Hospital, Hallym University College of Medicine. The trial plans to enroll 90 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology