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Real world study on endoscopic cryoablation for the treatment of urothelial tumors

Real world study on endoscopic cryoablation for the treatment of urothelial tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091372
Enrollment
Unknown
Registered
2024-10-28
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

Urothelial carcinoma

Interventions

Patients with urothelial carcinoma undergoing endoscopic cryoablation therapy:NA
Patients with urothelial carcinoma undergoing routine surgical treatment:NA

Sponsors

Department of Urology, Huashan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) From January 2019 to May 2024, the patient was clinically diagnosed as bladder cancer or renal pelvis and ureter cancer in Huashan Hospital affiliated to Fudan University; (2) The patient's histological diagnosis is urothelial carcinoma (allowing for any percentage of histological variation); (3) Age range: 18-85 years old, male or female not limited; (4) Patients participating in clinical trials (provided that the trial results have been published), patients receiving treatment according to standard treatment procedures, and patients receiving combination therapy using endoscopic cryoablation are all included in the study scope;

Exclusion criteria

Exclusion criteria: (1) The patient did not receive surgical treatment; (2) The patient's clinical and pathological data is incomplete; (3) The patient refused to use their own clinical data for the analysis of this clinical study; (4) The patient's postoperative pathology ruled out the diagnosis of urothelial carcinoma; (5) Researchers believe that there are other situations that are not suitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
overall survival of 2 years;

Secondary

MeasureTime frame
progression free survival of 2 years;Incidence of postoperative adverse events;Quality of life score;Quality-adjusted life years;

Countries

China

Contacts

Public ContactHaowen Jiang

Fudan University Affiliated Huashan Hospital

haowj_sh@fudan.edu.cn+86 181 2118 6785

Outcome results

None listed

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