CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 310 target
Drug / intervention
Biological sample +1 morebiological
Likely dose
Biological sample 10mLfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01339975
NCT01339975N/ACompleted

Level of Expression and Prognostic Value of CXCL4, CXCL4L1 and CXCR3 in Renal Cell Carcinoma

University Hospital, Bordeaux·observational·Posted Apr 21, 2011·Updated Aug 5, 2019

In Brief

An observational study evaluating Biological sample for Carcinoma and 4 related conditions. Completed, enrolled 310 participants across 1 site.

Detailed Summary

Despite novel treatment options, Renal Cell Carcinoma (RCC) has been characterized by a constant increase in its mortality and consequently requires an important involvement in translational research. The aim of this study is to evaluate the interest of CXCL4, CXCL4L1 and CXCR3 as biomarkers in localized, locally advanced or metastatic RCC. Indeed these chemokines have shown anti-angiogenic and anti-tumor properties in experimental models and may be particularly interesting for prognostic and predictive purposes.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesFrance
Collaborators--

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedApr 21, 2011
Enrollment StartJun 6, 2011
Primary CompletionMay 1, 2014
Study CompletionMay 1, 2019
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 15.2 years ago

Interventions

Biological samplebiological

2 blood samples of 10mL + one urine sample * on pre-operative d-1/d, post-operative d1 and d5(+/-2), * one month post-operative, * at the end of the study in the absence of disease progression or at the date of recurrence or progression if the case arises.

Biological samplebiological

2 blood samples of 10mL + one urine sample * before starting the therapy * at first therapeutic evaluation (2 or 3 months depending on the treatment chosen) * at the end of the study or at the date of disease progression.