Actively Recruiting

Age: 18Years +
All Genders
NCT05089747

CIRculating CANcer MAster-Protocol

Led by Hospices Civils de Lyon · Updated on 2023-07-24

6000

Participants Needed

5

Research Sites

1303 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This exploratory study will focus on the development of the analyses of blood biomarkers to better understand the circulating biomarkers associated with cancer diagnosis, treatment efficacy and progressive disease

CONDITIONS

Official Title

CIRculating CANcer MAster-Protocol

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult (over 18 years old)
  • Have social security insurance
  • Diagnosed with any solid cancer by histopathology or cytology
  • Blood sampling required as part of standard care
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Refusal to participate
  • No blood sampling required as part of standard care
  • Hemoglobin less than 7 g/dl (less than 9 g/dl if history of respiratory or cardiovascular disease)
  • Received heterologous blood transfusion within the last 48 hours
  • Weigh under 20 kg

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 5 locations

1

Service de Pneumologie Hôpital Louis Pradel / Groupement Hospitalier Est

Bron, France, 69500

Actively Recruiting

2

Service de Pneumologie Hôpital Croix-Rousse / Groupement Hospitalier Nord

Lyon, France, 69004

Actively Recruiting

3

Service de Pneumologie Aigue Spécialisée et Cancérologie Thoracique Hôpital Lyon-Sud / Groupement Hospitalier Sud

Pierre-Bénite, France, 69310

Actively Recruiting

4

Oncologie médicale Hôpital Lyon-Sud / Groupement Hospitalier Sud

Pierre-Bénite, France, 69495

Actively Recruiting

5

Service de dermatologie Hôpital Lyon-Sud / Groupement Hospitalier Sud

Pierre-Bénite, France, 69495

Actively Recruiting

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Research Team

S

Sebastian Couraud, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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