- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03868527
The ARCAN Database is Used for Retrospective Non-interventional Research Projects. The Database Collects Clinical and Laboratory Data From Patients With Lymphoid Malignancies. The Database Doesn't Require Biological Sample of Patients, it Records Only Information Based on the Patients' Medical File. (Arcan database)
March 8, 2019 updated by: Hospices Civils de Lyon
To identify the diagnostic and therapeutic approach (efficacy and toxicity) of patients with lymphoid malignant hemopathy who are managed in the hematology department.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
13000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Gilles Salles, MD
- Phone Number: +33 0478864307
- Email: gilles.salles@chu-lyon.fr
Study Contact Backup
- Name: Marion Choquet
- Email: marion.choquet@chu-lyon.fr
Study Locations
-
-
-
Pierre-Bénite, France
- Recruiting
- Hopital Lyon Sud
-
Contact:
- Gilles Salles, MD
- Phone Number: +33 0478864307
- Email: gilles.salles@chu-lyon.fr
-
Principal Investigator:
- Gilles Salles, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients followed for lymphoid malignant hemopathy in Lyon Sud Hospital
Description
Inclusion Criteria:
- Patients followed for hematological diseases in Lyon Sud Hospital
Exclusion Criteria:
- Patients who doesn't have hematological diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Hematological diseases
Cohort of patients followed for lymphoid malignant hemopathy in Lyon Sud Hospital
|
Data collection for biostatistical analysis about hematological diseases
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Progression-free survival
Time Frame: 730 days
|
Period between the end of the first treatment and the first confirmed relapse of lymphoma of patients who have received treatment to treat their lymphoma.
|
730 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gilles SALLES, MD, Hospices Civils de Lyon
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2003
Primary Completion (Anticipated)
December 31, 2025
Study Completion (Anticipated)
December 31, 2025
Study Registration Dates
First Submitted
February 26, 2019
First Submitted That Met QC Criteria
March 8, 2019
First Posted (Actual)
March 11, 2019
Study Record Updates
Last Update Posted (Actual)
March 11, 2019
Last Update Submitted That Met QC Criteria
March 8, 2019
Last Verified
March 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ARCAN Database
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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