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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01831609
Other study ID # 2011-07-089-013
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 31, 2011
Est. completion date December 2024

Study information

Verified date June 2022
Source Samsung Medical Center
Contact Jeeyun Lee, MD
Phone 822-3410-3459
Email jyun.lee@samsung.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To prospectively collect ascites, pleural fluid, circulating tumor cells and derived primary cultures from metastatic cancer patients. The specimens will be analyzed using DNA/RNA/proteomic approaches.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 2024
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Patients with histologically confirmed gastrointestinal, genitourinary, sarcoma, rare cancer 2. Written informed consent 3. body fluid derived from cancer, available for drainage and collection Exclusion Criteria: - patients who do not give informed consent form for research use of biomaterials/biospecimens

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Samsung Medical Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Biomarker analyses to predict treatment response in metastatic cancer Using patient derived tumor cells, predictive biomarker analyses (DNA, RNA protein levels etc) will be assessed. 3 year
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