Clinical trial Recruiting at 1 site Observational Ages 18 and up

Treatment patterns for managing high blood pressure in Brazil's public primary care system

Official title: Clinical Landscape of Epidemiology and Assessment of Results in Hypertension

Run by AstraZeneca · NCT07361276 · Data updated 2026-11-12

This project uses past medical records to see how adults with high blood pressure are treated in Brazil's public primary care system.

More Hypertension trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment15000 (estimated)
SponsorAstraZeneca
Industry-sponsored
Locations1 site (Florianópolis)
StatusRecruiting
StartedMarch 31, 2026
Main results expectedNovember 30, 2026
Study endsNovember 30, 2026
Registry record updatedOctober 22, 2026
Trial IDNCT07361276 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older with a recorded hypertension diagnosis or at least two consecutive high blood pressure readings in the participating municipalities' EMRs and with at least six months of continuous follow-up in the same municipality are the ideal candidates for inclusion.

Probably not a fit

People whose records are incomplete, not traceable, or who receive care outside the participating municipalities are excluded and unlikely to benefit directly from this analysis.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This retrospective observational cohort uses routinely collected electronic health records from five Brazilian municipalities participating in the epHealth Primary Care Solutions platform to characterize treatment patterns for hypertension. Adults (≥18) will be identified by recorded hypertension diagnoses or by at least two consecutive blood pressure measurements ≥140/90 mmHg within 30 days and followed for a minimum of six months. Primary outcomes focus on diagnostic and therapeutic clinical inertia, including timing of treatment changes and alignment with national guideline recommendations rather than testing an intervention. The design leverages existing EMR data to capture real-world practice across diverse socio-demographic and healthcare settings within Brazil's public primary care system.

Why it matters

Potential benefit: If successful, the findings could reveal gaps and delays in hypertension care and guide changes to improve blood pressure control across Brazil's public primary care system.

How similar studies have gone: Similar retrospective analyses of electronic health records have previously documented clinical inertia and treatment gaps in hypertension care, so the approach is well-established though findings vary by setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥18 years at the time of Hypertension diagnosis
* Hypertension diagnosis as retrieved from registered ICD codes or CIAP Codes (primary care codes) in the EMR , OR At least two blood pressure measurements ≥140/90 mmHg during the study period. The blood measurements should be consecutive and obtained within a 30 days period.
* Continuous follow-up in the same municipality for at least 6 months after index measurement.
* Availability of structured EMR data including clinical encounters, diagnoses, and prescriptions

Exclusion Criteria:

\- Patients with incomplete data or not traceable in the registration systems

Where it's running

  • Research Site
    Florianópolis, Brazil
    Recruiting

Study contacts

  • Principal investigator: Julia Machline Carrion, Medical — EpHealth Soluções em Tecnologia da Informação Ltda
  • Study coordinator: AstraZeneca Clinical Study Information Center
  • Email: information.center@astrazeneca.com
  • Phone: 1-877-240-9479

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.