Study Evaluating Renal Cell Carcinoma Risk Factors

NCT ID: NCT00927043

Last Updated: 2011-11-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

145 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-05-31

Study Completion Date

2011-09-30

Brief Summary

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This is an epidemiological, prospective, multicenter study designed to identify the pre-treatment clinical, molecular and genetic prognostic factors associated with progression free survival in patients naïve to renal cell carcinoma (RCC) treatment.

Detailed Description

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invitation to volunteer

Conditions

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Carcinoma, Renal Cell

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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1

Epidemiological study according to clinical practice

Intervention Type OTHER

Epidemiological study according to clinical practice.

Interventions

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Epidemiological study according to clinical practice

Epidemiological study according to clinical practice.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Treatment naïve patients with proven advanced RCC will be evaluated. (Except surgery or radiotherapy)
* =18 years, any gender.
* Patients with advanced Renal Cell Carcinoma and treatment naïve.

Exclusion Criteria

* Patients who have already initiated any kind of specific therapy for the treatment of RCC.2.
* Patients with other neoplasias different from RCC (current or past).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Pamplona, Navarre, Spain

Site Status

Countries

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Spain

Related Links

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Other Identifiers

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B1771010

Identifier Type: -

Identifier Source: secondary_id

3066K1-4433

Identifier Type: -

Identifier Source: org_study_id