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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01651013
Other study ID # CALLAS
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date October 2010
Est. completion date December 2023

Study information

Verified date March 2023
Source National Cancer Institute, Naples
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to describe the treatments received and outcomes of patients with metastatic colorectal cancer, what percentage of these patients have K-Ras mutation of the tumor, and to describe the costs of treatments. Information will also be collected regarding risk factors, variables among treatment centers and patients, and explorative analyses will be done to try to identify factors that impact prognosis and factors that predict tolerability and response to treatment.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 500
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Histologic diagnosis colorectal carcinoma - Metastatic disease - Signed informed consent Exclusion Criteria: - Prior treatment of metastatic colorectal cancer - Refusal or incapability of providing informed consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy A.O.G. Rummo Benevento
Italy Istituto Nazionale dei Tumori , Oncologia Medica - Dipartimento Entero-proctologico Napoli
Italy Ospedale Civile Umberto I Nocera Inferiore
Italy C:R.O. Regione Basilicata Ospedale Giustino Fortunato Rionero in Vulture

Sponsors (1)

Lead Sponsor Collaborator
National Cancer Institute, Naples

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Other metastatic colorectal cancer treatments used in clinical practice, according to participating center 2 years
Other patient outcome according to K-Ras status two years
Other estimated costs per treatment per center 2 years
Other disease outcome per patient per treatment received 2 years
Other factors that influence patient prognosis exploratory analyses 2 years
Other predictive factors for response to treatment exploratory analyses 5 years
Primary percentage of patients enrolled in a clinical trial two years
Primary percentage of patients who undergo K-Ras mutation study 2 years
Primary Percentage of patients with K-Ras mutation 2 years
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