CARE - Quality Improvement in Cardiovascular Secondary Prevention in Primary Care, Through Delegation of Consultations to the Nurse.
NCT ID: NCT00713960
Last Updated: 2012-01-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
2193 participants
OBSERVATIONAL
2008-04-30
2010-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation Research of a National Accreditation and Improvement Programme for General Practice
NCT00791362
Patient-reported Outcomes After Percutaneous Coronary Intervention
NCT03810612
One Heart to Care for
NCT04753398
Safety and Effectiveness of Drug up Titration by Nurses Specialized in Heart Failure (HF) Patients
NCT02546856
Can Diagnostics and Pharmacological Prescriptions in Patients With Heart Failure be Improved in General Practice?
NCT01476566
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
Patients in secondary prevention of cardiovascular disease in primary care
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* According to the general practitioners appraisal, patients who suffer from severe co morbidity can be excluded as well.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
AstraZeneca
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Henrik Ommen, MD
Role: STUDY_CHAIR
Lægerne i Løgumkloster I/S, Denmark
Dorte Knudsen
Role: STUDY_CHAIR
Lægerne Sønderåparken, Denmark
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Research Site
Albertslund, , Denmark
Research Site
Arhus C, , Denmark
Research site
Assens, , Denmark
Research Site
Billund, , Denmark
Research Site
Brabrand, , Denmark
Research Site
Elsinore, , Denmark
Research Site
Erslev, , Denmark
Research Site
Esbjerg, , Denmark
Research Site
Faaborg, , Denmark
Research Site
Gentofte Municipality, , Denmark
Research Site
Give, , Denmark
Research Site
Greve, , Denmark
Research Site
Hadsund, , Denmark
Research Site
Hedehusene, , Denmark
Research Site
Hillerød, , Denmark
Research Site
Hinnerup, , Denmark
Research Site
Hjallerup, , Denmark
Research Site
Hjørring, , Denmark
Research Site
Hobro, , Denmark
Research Site
Holaek, , Denmark
Research Site
Holstebro, , Denmark
Research Site
Hornsyld, , Denmark
Research Site
Horsens, , Denmark
Research Site
Hørning, , Denmark
Research Site
Karup, , Denmark
Research Site
Kbh. O, , Denmark
Research Site
Kerteminde, , Denmark
Research Site
Kjellerup, , Denmark
Research Site
Klarup, , Denmark
Research site
Kobenhavn V, , Denmark
Research Site
Kolding, , Denmark
Research Site
Kolding C, , Denmark
Research Site
Kongens Lyngby, , Denmark
Research Site
København Ø, , Denmark
Research Site
Køge, , Denmark
Research Site
Lemvig, , Denmark
Research Site
Lystrup, , Denmark
Research Site
Maribo, , Denmark
Research Site
Nivå, , Denmark
Research Site
Næstved, , Denmark
Research Site
Odense C, , Denmark
Research Site
Pandrup, , Denmark
Research Site
Randers, , Denmark
Research Site
Ringsted, , Denmark
Research Site
Roskilde, , Denmark
Research Site
Rungsted Kyst, , Denmark
Research Site
Rødding, , Denmark
Research Site
Silkeborg, , Denmark
Research Site
Skælskør, , Denmark
Research Site
Solrød Strand, , Denmark
Research Site
Stege, , Denmark
Research Site
Struer Municipality, , Denmark
Research Site
Svendborg, , Denmark
Research Site
Svinninge, , Denmark
Research Site
Sønder Felding, , Denmark
Research Site
Sønderborg, , Denmark
Research Site
Thisted, , Denmark
Research Site
Tune, , Denmark
Research Site
Vamdrup, , Denmark
Research Site
Varde, , Denmark
Research Site
Vejen Municipality, , Denmark
Research Site
Vejle, , Denmark
Research Site
Vestervig, , Denmark
Research Site
Viborg, , Denmark
Research Site
Viby J, , Denmark
Research Site
Vivild, , Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NIS-CDK-DUM-2008/1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.