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Clinical Trials/NCT01978925
NCT01978925CompletedNot Applicable

Effectiveness Pharmaceutical Care at Discharge in the Emergency Department: a Randomized Controlled Trial

Hospital Moinhos de Vento2 sites in 1 country380 target enrollmentStarted: November 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
380
Locations
2
Primary Endpoint
Medication Adherence

Study Overview

Brief Summary

The purpose of this study is to evaluate the effectiveness of pharmaceutical care, compared to usual care, in patient discharge in an emergency department in patients with hypertension and/or diabetes mellitus type 2.

Detailed Description

This is a randomized controlled, single-center study, with blinding of outcome assessors. A pilot study with ten patients was previously conducted in order to test study logistics and data collection instruments. Participants will be recruited from a public ED at Restinga district in Porto Alegre, southern Brazil.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Blood pressure inadequate control (systolic blood pressure ≥ 160 or diastolic blood pressure ≥ 100 mmHg) or
  • Diabetes mellitus inadequate Control( ≥ 200 mg/dL) or hypoglycemia moderate or severe
  • Be referred to clinical care.

Exclusion Criteria

  • < 18 years
  • Not resident of Porto Alegre
  • Diabetes mellitus type I
  • Unable to answer the questionnaire or to sign the informed consent form
  • Hospital admission

Outcomes

Primary Outcomes

Medication Adherence

Time Frame: Two months

Outcome of interest: High Adherence According to the Brief Medication Questionnaire and Morisky-Green Test

Secondary Outcomes

  • Quality of Life(Two months)
  • Blood Pressure Control(Two months)
  • Glycated hemoglobin (HbA1C) for diabetic patients(two months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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