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A Quality Ensuring Project With Focus On Patients With Cardiovascular Diseases As Well As Type 2 Diabetes.

Patient And Physician Alliance -Guideline Education Treatment Optimization

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00415428
Enrollment
2776
Registered
2006-12-22
Start date
2007-01-31
Completion date
2008-09-30
Last updated
2021-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 2, Heart Diseases

Brief summary

The overall objective is to increase the adherence to national guidelines for patients with established CVD and/or Type 2 diabetes by means of repeated post-graduate educational meetings and regular evaluation of the optimisation initiatives, demonstrated by improvement of goal attainment in general practice.

Interventions

BEHAVIORALPatient adherence to national educational guidelines.

Sponsors

Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subjects had to meet all of the inclusion criteria to be eligible for enrollment into the study. The following subjects qualify for inclusion in the study: * Subjects for whom measurement of total cholesterol, low density lipoprotein (LDL) cholesterol, blood pressure (BP) and glycosylated hemoglobin (HbA1c) was planned independently of this observational study and for whom baseline values were or became available. * Subjects with known CVD diagnosed \> or = 6 months before inclusion * Previous myocardial infarction * Ischemic heart disease (stable and unstable angina pectoris) * Ischemic apoplexy * Peripheral arterial disease * And/Or * Subjects with T2D diagnosed \> or = 6 months before inclusion * At least 50% of the subjects had to have CVD as the primary diagnosis. It was allowed for a secondary diagnosis to be \<6 months before inclusion.

Exclusion criteria

* Subjects presenting with any of the following were not to be included in the study: * Life expectancy of \< or = 2 years * Unable/unwilling to understand/follow instructions * Taking part in a clinical study involving an investigational drug * Followed by a specialist for their CVD and/or T2D at the time of inclusion in the study

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026