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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03789682
Other study ID # FUSCC-URO1201-2018-1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date January 1, 2028

Study information

Verified date February 2020
Source Fudan University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This research is designed to investigate the prognostic and predictive value of CD155 in muscle invasive bladder cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date January 1, 2028
Est. primary completion date January 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- patients with non-metastatic muscle invasive bladder cancer

- pathology confirmed urothelial carcinoma

- underwent cystectomy and pelvic lymph node dissection

Exclusion Criteria:

- not enough tissue for immunohistochemistry

- patients with a second neoplasm

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Adjuvant chemotherapy
adjuvant chemotherapy using Gemcitabine plus Cisplatin

Locations

Country Name City State
China Fudan University Shanghai Cancer Center Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Fudan University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recurrence free survival Time to recurrence or metastasis 2018.1.1-2023.12.31
Secondary Overall survival Time to death 2018.1.1-2028.1.1
Secondary Benefit from neoadjuvant chemotherapy response to neoadjuvant chemotherapy 2018.1.1-2028.1.1
Secondary Benefit from adjuvant chemotherapy Survival analysis grouped by adjuvant chemotherapy 2018.1.1-2028.1.1
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