Observational Pharmaco-Epidemiology Research & Analysis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0+
SponsorEpividian

About this trial

Greater advances are needed in two separate but related areas in healthcare: 1) the Clinical Decision Support Systems that complement the EHR use in support of routine patient care, population management and disease management; and 2) the use of the point-of-care observational data from the provider-patient encounter that support realworld medical research and healthcare quality measure assessment. Real-world evaluations of treatments of chronic diseases in the context of comorbid conditions and special populations (minorities, women, mentally ill, and those with addiction) are limited. The purpose of the OPERA database is to help address this unmet need in clinical research.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients who are treated in the practices who enroll and participate in the study

Patients whose treatment is documented in the practice's electronic health record system

Disqualifiers

Patients who opt out of OPERA

Trial population

The patient population includes a diverse group of individuals treated in ambulatory practice with a focus on those living with chronic disease.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Non-interventional (observational only)

    Other intervention

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Virologic response to therapy

HIV-1 PCR laboratory value ("viral load") quantifies the amount of HIV-1 copies in plasma per mL. The baseline viral load is compared to viral load after 1 year of antiretroviral therapy.

Time frame
1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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