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NCT07272603

Bladder Perfusion of Plasma-Activated Saline for Bladder Cancer

Not yet recruiting EARLY_PHASE1 Last updated 9 December 2025
What this trial tests

EARLY_PHASE1 trial testing Plasma-Activated Saline Solution (PASS) Bladder Instillation in Bladder (Urothelial, Transitional Cell) Cancer in 5 participants. Not yet recruiting.

Timeline
15 December 2025
Primary endpoint
15 February 2026
15 February 2026

Quick facts

Lead sponsorQilu Hospital of Shandong University
PhaseEARLY_PHASE1
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment5
Start date15 December 2025
Primary completion15 February 2026
Estimated completion15 February 2026

Drugs / interventions tested

Conditions studied

Sponsor

Qilu Hospital of Shandong University

Who can join

Adults 18 to 75, any sex, with Bladder (Urothelial, Transitional Cell) Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This preliminary clinical study evaluates the safety and initial efficacy of a novel therapy called Plasma-Activated Saline Solution (PASS) for bladder cancer patients. The study involves a one-week course of PASS administered via bladder infusion in five pre-surgical patients, using imaging and pathology analyses to assess tumor shrinkage and cancer cell death, while closely monitoring for any adverse reactions to explore the therapy's future potential.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Bladder (Urothelial, Transitional Cell) Cancer

Currently open trials in the same condition.

Other Qilu Hospital of Shandong University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07272603.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing