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Clinical Trials/ISRCTN16857539
ISRCTN16857539Active, not recruiting未知

Validation of home blood pressure monitors in patients with atrial fibrillation

niversity of Birmingham0 sites33 target enrollmentStarted: January 20, 2016Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Active, not recruiting
Enrollment
33

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
All

Inclusion Criteria

  • 1. Initial diagnosis of atrial fibrillation, confirmed by 12 lead electrocardiogram and judged by primary care physician to be eligible to participate
  • 2. Aged 25 years or over
  • 3. Recruitment blood pressures should be in the range 90–180mmHg for SBP and 40–130mmHg for DBP. If patients with blood pressures outside these ranges are available they may be included but only to a maximum of four such pressures. The number of subjects in each recruitment range (SBP: low <130mmHg, medium 130160mmHg, high >160mmHg; DBP: low <80mmHg, medium 80100mmHg, high >100mmHg) must be between 10 and 12 subjects.

Exclusion Criteria

  • Three failed attempts in machine measurement.

Investigators

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