Sign in

NCT03126214CompletedPhase 4

Improving Stroke Prevention in Atrial Fibrillation Through Pharmacist Prescribing

Improving Stroke Prevention in Atrial Fibrillation Through Pharmacist Prescribing: Program for the Identification of 'Actionable' AF (PIAAF) Rx Study

Source: ClinicalTrials.gov · Last updated 5 Jan 2024

Brief summary (registry, in English)

The purpose of this study is to compare the effectiveness of prescribing oral anticoagulation therapy by pharmacist intervention compared to enhanced usual care in participants with unrecognized AF and/or known AF but not taking blood thinners.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
79 (actual)
First submitted
12 Apr 2017
Start date
1 Feb 2018
Primary completion date
1 Jul 2022
Lead sponsor
University of Alberta
NCT number
NCT03126214

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 79
  • From 1 Feb 2018 to the primary completion date, 1 Jul 2022
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Uncontrolled hypertension (defined as average SBP ≥ 160 mmHg \[2 readings taken at time of screening\]).
  • End stage renal disease (CrCl \< 15 ml/min)
  • Valvular Heart Disease including those with prosthetic valve, mitral stenosis (moderate to severe) or valve repair.
  • History of "Major Bleeding" at any point (defined as overt bleeding at a critical site including intracranial, intraspinal, intraocular, pericardial, or retroperitoneal; or bleed requiring hospitalization).
  • Severe cognitive impairment (defined as score ≥ 5 on the Short Portable Mental Status Questionnaire)

Other

  • Excess alcohol intake (males: ≥ 28 units/week, females: ≥ 21 units/week. One unit of alcohol = 8 oz beer, 1 oz hard liquor or 4 oz wine).
  • Intracranial bleed at any point.
  • Foreshortened life-expectancy or severe comorbidities precluding study follow-up period
  • Unable to read/understand English

Who the study is looking for

  • Age ≥ 65 years with one additional stroke risk factor (hypertension, diabetes, heart failure history of or left ventricular ejection fraction \<0.40), previous stroke or transient ischemic attack).
  • Atrial fibrillation and not on oral anticoagulation (OAC) therapy but eligible
  • Atrial fibrillation on sub-optimal OAC

Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alberta
Coordinator of this site? Confirm its status
EdmontonCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.