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Study identifier: NCT06167057 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

POST URS Chemotherapy Instillation

Condition: UTUC  ·  Sponsor: Carmel Medical Center

PhaseNA
Planned participants264
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this study is to evaluate the safety and oncological outcomes of single chemotherapy bladder instillation following endoscopic treatment for UTUC in UTUC suspected patients .The main aim is to determine the efficacy of a single, post URS, chemotherapy bladder instillation to reduce IVR. Participants will be given single chemotherapy bladder instillation within 24h following ureteroscopy and will follow routine follow-up for IVR which will include white light cystoscopy ;patients with suspected IVR (based on either imaging or cystoscopy) will undergo TURBT.

This description comes directly from the study's public registry record.

Talk to the study team

Yuval Freifeld, Dr  ·  +972-4-8250843  ·  yuvalfr@clalit.org.il

Always discuss trial participation with your own doctor first.

Locations (10)

Assuta Ashdod HospitalAshdod, IsraelRecruiting
Soroka University Medical CenterBeersheba, IsraelRecruiting
Shamir Medical CenterBe’er Ya‘aqov, IsraelRecruiting
Bnai Zion Medical CenterHaifa, IsraelRecruiting
Carmel Medical CenterHaifa, IsraelRecruiting
Rambam Health Care CampusHaifa, IsraelRecruiting
Rabin Medical Center - Beilinson and HasharonPetah Tikva, IsraelRecruiting
Kaplan Medical CenterRehovot, IsraelRecruiting
Ziv Medical CenterSafed, IsraelRecruiting
Tel Aviv Sourasky Medical Center - IchilovTel Aviv, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06167057