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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04952103
Other study ID # Fudan-CUP-003
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 18, 2021
Est. completion date June 18, 2024

Study information

Verified date June 2021
Source Fudan University
Contact Xin Liu
Phone 13761503356
Email jeanettexin@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is a prospective, real world study.The objective is to observe the diagnosis and first-line treatment of Chinese patients with cancer of unknown primary, and collect the clinicopathological characteristics, treatment outcomes, survival and other data of the patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date June 18, 2024
Est. primary completion date June 18, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Had a diagnosis of cancer of unknown primary (CUP) after a standard evaluation . - Prepared to receive first-line therapy for CUP Exclusion Criteria: - Patients who had previously received systemic therapy for CUP - Previous history of other cancers, except cervix cancer or basal cell carcinoma of the skin that has been cured - The investigator considered that there were contraindications to treatment or were not appropriate to participate in this study

Study Design


Intervention

Other:
no intervention
The patient's treatment is determined by the physician in charge according to the patient's clinical situation and relevant guidelines, without additional intervention.

Locations

Country Name City State
China Fudan University Shanghai Cencer 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 Progression-free survival (PFS) 8 months
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