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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06239129
Other study ID # 000001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2006
Est. completion date December 31, 2022

Study information

Verified date January 2024
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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/


Description:

Please consult cohort description in: https://pubmed.ncbi.nlm.nih.gov/35028991/ https://pubmed.ncbi.nlm.nih.gov/26798472/


Recruitment information / eligibility

Status Completed
Enrollment 3200000
Est. completion date December 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers
Gender All
Age group 0 Years to 110 Years
Eligibility Inclusion Criteria: For both cohorts: Be a resident of Stockholm during 2006-2021, of all ages For the primary cohort: To have undertaken at least one test of serum creatinine or albuminuria during 2006-2021. If this condition is met, we will then extract a broad range of laboratory tests For the secondary cohort: Anyone not undertaking a test of serum creatinine or albuminuria will conform the secondary cohort. In this cohort we will not extract any other laboratory test, but will obtain the rest of healthcare information Exclusion criteria: None

Study Design


Intervention

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

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Karolinska Institutet Region Stockholm

Outcome

Type Measure Description Time frame Safety issue
Primary Adverse health events by levels of kidney function multiple outcomes evaluated such as cardiovascular events, fractures, dementia, cancer, etc, all of them based on claims data and/or laboratory data 2006-2021
Primary Safety and efficacy of medications by levels of kidney function multiple outcomes evaluated depending on the treatments of interest, all of them based on claims data and/or laboratory data 2006-2021
Primary Effect of medications or conditions on kidney function decline Evaluation of changes in kidney function over time upon occurrence of a certain condition (i.e., heart failure or covid19 infection) or initiation of a specific medication 2006-2021
Secondary Adverse health events associated to laboratory abnormalities Same as primary objectives but for other laboratory abnormalities different from kidney function measures 2006-2021
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