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Clinical Study of Plasma in Bladder Perfusion Therapy for Non-Muscle-Invasive Bladder Cancer

Clinical Study of Plasma in Bladder Perfusion Therapy for Non-Muscle-Invasive Bladder Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112525
Enrollment
Unknown
Registered
2025-11-16
Start date
2025-11-16
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Nonmuscle invasive bladder cancer

Interventions

Experimental Group:Intravesical perfusion of plasma-activated normal saline

Sponsors

The First Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Those with a pathological diagnosis of non-muscle-invasive bladder urothelial carcinoma. 2. Those without lymph node or distant metastasis confirmed by imaging examinations.

Exclusion criteria

Exclusion criteria: 1. It is known or possible that a bladder tumor has metastasized from another organ; 2. Patients who cannot tolerate or are not suitable for TURBT; 3. Patients in the acute infection stage or with systemic infection; 4. Suffering from other tumors; 5. Patients who have previously received intravesical treatment; 6. Patients with severe coagulation dysfunction or insufficiency of vital organs such as the heart, brain and lungs; 7. Patients who did not have regular follow-up visits or follow-ups after surgery and have lost contact.

Design outcomes

Primary

MeasureTime frame
Incidence of dose-limiting toxicity;

Secondary

MeasureTime frame
Incidence of dose-limiting toxicity;

Countries

China

Contacts

Public ContactYang Xiaojian

The First Affiliated Hospital of Air Force Medical University

xiaojianyangxjh@163.com+86 186 8182 6607

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026