The Stockholm CREAtinine Measurements Project
NCT06239129 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3200000
Last updated 2024-02-02
Summary
The Stockholm CREAtinine Measurements (SCREAM) project is a healthcare utilization cohort including, at present, all adult residents in Stockholm between 2006 and 2021. The region of Stockholm had a population of 2.3 million citizens in 2021and provides universal healthcare with a single unified health-system. Administrative databases with complete information on socidemographic data, healthcare use, diagnoses and therapeutic/surgical procedures, and vital status were enriched with performed laboratory tests, dispensed prescriptions at Swedish pharmacies and validated kidney replacement therapy endpoints. Registries were linked and de-identified by the Swedish National Board of Welfare and are considered to have no or minimal loss to follow-up. Because the study utilized de-identified data, it was deemed not to require informed consent and was approved by the regional ethical review boards and the Swedish National Board of Welfare.
For detailed description of available data and linked registers please consult:
https://pubmed.ncbi.nlm.nih.gov/35028991/
Conditions
- Chronic Kidney Diseases
- Acute Kidney Injury
- Diabetes Mellitus
- Cardiovascular Diseases
- Hypertension
Interventions
- DRUG
-
Initiation of specific medications
multiple therapies studied within this database
- PROCEDURE
-
Undertaking of specific procedures
multiple procedures/surgeries studied within this database
- DIAGNOSTIC_TEST
-
Abnormalities in specific laboratory tests
multiple abnormalities in laboratory values (i.e. CRP, cholesterol, eGFR, potassium) studied within this database
Sponsors & Collaborators
-
Region Stockholm
collaborator OTHER_GOV - lead OTHER
Principal Investigators
-
Juan J Carrero, Prof · Karolinska Institutet
Eligibility
- Min Age
- 0 Years
- Max Age
- 110 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-01-01
- Primary Completion
- 2021-12-31
- Completion
- 2022-12-31
- FDA Drug
- Yes
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