ITMO public health
Last update : 12/05/2024 | Version : 1 | ID : 74126
| General | |
| Identification | |
| Detailed name | A non-interventional study to assess the hemoglobin level depending on the comorbidity index in chronic kidney disease (CKD) patients not on dialysis treated with Mircera® |
| Sign or acronym | COMETE |
| CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation | ML28145 |
| General Aspects | |
| Medical area |
Urology, andrology and nephrology |
| Study in connection with Covid-19 |
No |
| Pathology (details) | Chronic Kidney Disease not on dialysis |
| Health determinants |
Iatrogenic Medicine |
| Keywords | MIRCERA® |
| Scientific investigator(s) (Contact) | |
| Name of the director | Roche Medical Data Center |
| Address | 4 cours de l'Ile Seguin - 92650 BOULOGNE-BILLANCOURT |
| data_sharing_france@roche.com | |
| Organization | Roche SAS |
| Collaborations | |
| Participation in projects, networks and consortia |
No |
| Funding | |
| Funding status |
Private |
| Governance of the database | |
| Sponsor(s) or organisation(s) responsible | Roche SAS |
| Organisation status |
Private |
| Presence of scientific or steering committees |
Yes |
| Additional contact | |
| Name of the contact | https://www.roche.fr/fr/innovation-recherche-medicale/data-sharing-portail-d-information-partage-des-donnees.html |
| Main features | |
| Type of database | |
| Type of database |
Study databases |
| Study databases (details) |
Cohort study |
| Database recruitment is carried out by an intermediary |
A selection of health institutions and services |
| Database recruitment is is made on the basis of: |
Medication(s) taken |
| Database recruitment is carried out as part of an interventional study |
No |
| Database objective | |
| Main objective |
Primary objective : Describe in current medical practice the evolution of hemoglobin levels during the 9-month follow-up in each subgroup defined by the Charlson comorbidity index.
Secondary objectives : - Describe the characteristics of patients treated with Mircera® in the total population and in the subgroups defined by the Charlson comorbidity index; - Describe the evolution of the hemoglobin level during the observation period according to the Liu comorbidity index and to ESA resistance factors; - Describe the changes in the Mircera® dosage during the observation period in the total population and in the subgroups defined by the Charlson comorbidity index; - Describe the safety profile of Mircera® during the observation period in the total population and in the subgroups defined by the Charlson comorbidity index. |
| Inclusion criteria |
Inclusion criteria :
- Patient >=18 years of age; - Patient with chronic kidney disease not on dialysis; - ESA-naive patients (not having received ESAs within the 6 months prior to inclusion); - Patients with hemoglobin level <10.0 g/dL at inclusion; - Patients for whom the treating physician has decided to initiate treatment with Mircera® for medical reasons prior to study start; - Patient having received both oral and written information about the study, without any objections for the use of his/her personal data. Non inclusion criteria : - Patients with functional renal transplant; - Patients participating in a clinical trial on anemia due to CKD. |
| Population type | |
| Age |
Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) Elderly (65 to 79 years) Great age (80 years and more) |
| Population covered |
Sick population |
| Pathology | N18 - Chronic kidney disease |
| Gender |
Male Woman |
| Geography area |
National |
| Data collection | |
| Dates | |
| Date of first collection (YYYY or MM/YYYY) | 2012 |
| Date of last collection (YYYY or MM/YYYY) | 2015 |
| Size of the database | |
| Size of the database (number of individuals) |
[500-1000[ individuals |
| Details of the number of individuals | 550 |
| Data | |
| Database activity |
Data collection completed |
| Type of data collected |
Clinical data Biological data |
| Clinical data (detail) |
Medical registration |
| Details of collected clinical data | Validation of inclusion and exclusion criteria - Dates of visits (or data of last contact with the patient) - Demographic - CKD history and evolution - Comorbidities - Most recent clinical and biological data - Previous and/or ongoing CKD treatments - Other specific treatments - Previous and/or ongoing anemia treatments - Treatment with Micera® - Adverses events - Reason for early study discontinuation. |
| Presence of a biobank |
No |
| Health parameters studied |
Health event/morbidity Health event/mortality Health care consumption and services |
| Care consumption (detail) |
Medicines consumption |
| Procedures | |
| Data collection method | eCRF |
| Classifications used | CDISC |
| Quality procedure(s) used | GCP/GVP |
| Participant monitoring |
Yes |
| Monitoring procedures |
Monitoring by contact with the referring doctor |
| Links to administrative sources |
No |
| Promotion and access | |
| Promotion | |
| Access | |
| Dedicated website | https://www.roche.fr/fr/innovation-recherche-medicale/data-sharing-portail-d-information-partage-des-donnees.html |
| Presence of document that lists variables and coding procedures |
Yes |
| Access to aggregated data |
Access on specific project only |
| Access to individual data |
Access on specific project only |
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