← Back to Clinical Trials
Recruiting NCT03293563

NCT03293563 UroCCR Database: French Research Network for Kidney Cancer -UroCCR

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT03293563
Status Recruiting
Phase
Sponsor University Hospital, Bordeaux
Condition Kidney Cancer
Study Type OBSERVATIONAL
Enrollment 30,000 participants
Start Date 2011-12
Primary Completion 2040-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Radical nephrectomy versus partial nephrectomy (according surgeon judgement)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 30,000 participants in total. It began in 2011-12 with a primary completion date of 2040-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Kidney cancer management has become increasingly complex with the diversification of treatment options and the integration of multidisciplinary care. To meet these challenges, the UroCCR network was established in France as a national registry and research platform dedicated to renal cancer. Funded by the French National Cancer Institute (INCa), UroCCR prospectively collects comprehensive real-world data on patient care and disease evolution, while systematically linking these records with annotated biological samples (plasma, urine, and both healthy and tumour tissues). For each case, more than one thousand variables may be recorded, covering clinical, imaging, and patient-reported information. More than a registry, UroCCR is a collaborative network of clinical and research professionals using a shared, evolving tool that supports rapid implementation of studies and fosters active knowledge generation. Unlike retrospective registries or sample-centred biobanks, UroCCR offers prospective, patient-focused inclusion and a wide scope of investigation-from translational and technological research to clinical evaluation and social sciences. It also supports multiple ancillary studies, including retrospective analyses and prospective clinical or observational trials, and operates under a structured governance system with recognised national and international labels. By combining a rigorously structured, multicentre dataset with linkage to the French national health data system (SNDS), the platform uniquely unites detailed clinical annotation with population-wide coverage, creating a high-value environment for advancing kidney cancer research and care.

Eligibility Criteria

Inclusion Criteria: * Adult patient with kidney cancer * Patient with no opposition to collection of its data for the study Exclusion Criteria: none

Contact & Investigator

Central Contact

Jean-Christophe BERNHARD, PHU

✉ jean-christophe.bernhard@chu-bordeaux.fr

📞 +33 (0)5 57 82 03 50

Principal Investigator

Jean-Christophe BERNHARD, PHU

PRINCIPAL INVESTIGATOR

University Hospital, Bordeaux

Frequently Asked Questions

Who can join the NCT03293563 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Kidney Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT03293563 currently recruiting?

Yes, NCT03293563 is actively recruiting participants. Contact the research team at jean-christophe.bernhard@chu-bordeaux.fr for enrollment information.

Where is the NCT03293563 trial being conducted?

This trial is being conducted at Brussels, Belgium, Angers, France, Bordeaux, France, Bordeaux, France and 11 additional locations.

Who is sponsoring the NCT03293563 clinical trial?

NCT03293563 is sponsored by University Hospital, Bordeaux. The principal investigator is Jean-Christophe BERNHARD, PHU at University Hospital, Bordeaux. The trial plans to enroll 30,000 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology