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Pharmaceutical Care in Emergency Department

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01978925
Acronym
AMPaRAR
Enrollment
380
Registered
2013-11-08
Start date
2013-11-30
Completion date
2014-12-31
Last updated
2015-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Hypertension, Medication Adherence

Keywords

Pharmaceutical care, Medication Adherence, Blood Pressure, Diabetes, Emergency

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.

Interventions

OTHERPharmaceutical care

The clinical pharmacist will provide a structured 30-minute intervention for enhancing their medication adherence. The recommendations include: discussion on hypertension and/or diabetes, risk of complications, prescribed drug therapy, correct use of medications and proper dosage, possible adverse effects, route of administration, schedule of administration and correct storage. The pharmacist will also emphasize the importance of lifestyle modifications. Printed educational material, with information on hypertension and/ or diabetes medications, including suggested lifestyle interventions was prepared to assist in the intervention and will be handed to patients in the end of the session.

Sponsors

Ministry of Health, Brazil
CollaboratorOTHER_GOV
Hospital Moinhos de Vento
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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 * Death

Design outcomes

Primary

MeasureTime frameDescription
Medication AdherenceTwo monthsOutcome of interest: High Adherence According to the Brief Medication Questionnaire and Morisky-Green Test

Secondary

MeasureTime frame
Blood Pressure ControlTwo months
Glycated hemoglobin (HbA1C) for diabetic patientstwo months
Quality of LifeTwo months

Other

MeasureTime frame
Fasting plasma glucose for diabetic patientsTwo months

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026