Database of patients with multiple myeloma at Institut Paoli-Calmettes
Institut Paoli Calmettes Multiple Myeloma Database
This study is creating a database of patients with multiple myeloma at Institut Paoli-Calmettes to help understand the disease better and improve how patients are treated.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 5000 (estimated) |
| Ages | 18 Years to 95 Years |
| Sex | All |
| Sponsor | Institut Paoli-Calmettes Academic / other |
| Locations | 1 site (Marseille, Bouches-du Rhône) |
| Trial ID | NCT02869555 on ClinicalTrials.gov |
What this trial studies
This observational study aims to create a comprehensive database of patients diagnosed with multiple myeloma at the Institut Paoli-Calmettes. The database will facilitate the collection of clinical data to better understand the disease and improve patient management. By analyzing this data, researchers hope to identify patterns and outcomes that can inform future treatment strategies. The study does not involve any specific interventions but focuses on data collection from existing patient records.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals diagnosed with multiple myeloma after January 1, 2008.
Not a fit: Patients diagnosed with multiple myeloma before January 1, 2008, will not benefit from this study.
Why it matters
Potential benefit: If successful, this database could enhance understanding of multiple myeloma and lead to improved treatment approaches for patients.
How similar studies have performed: Other studies utilizing patient databases for multiple myeloma have shown success in identifying treatment patterns and outcomes, indicating that this approach is validated.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Multiple myeloma diagnosis Exclusion Criteria: * Diagnosis before 1st january 2008
Where this trial is running
Marseille, Bouches-du Rhône
- Institut Paoli-Calmettes — Marseille, Bouches-du Rhône, France (Recruiting)
Study contacts
- Study coordinator: Dominique Genre, MD
- Email: drci.up@ipc.unicancer.fr
- Phone: 0033491223778
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.