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OpenTrials
Completed

NCT Number: NCT02805270

Impact of Medication Reconciliation Intervention on the Rate of Preventable Adverse Drug Events (ADEs) and Healthcare Utilization

The implementation of a medication reconciliation intervention including: medication reconciliation on admission and discharge, bedside medication counselling and take-home medication list, on the development of adverse drug events within 30 days post discharge as primary outcome. Secondary outcome is the evaluation of its impact on health care resource utilization

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

This is a randomized controlled trial in 587 patients randomized to intervention and usual care. The intervention is medication reconciliation on admission and discharge, bedside medication counselling and take-home medication list. Usual care is ward pharmacy practice. The primary outcomes are preventable and potential adverse drug events at 30 days post discharge. The secondary outcome is health care utilization: length of stay, emergency room visits, unplanned hospital visits, readmissions and travel abroad to seek medical attention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • admitted to one of the two medical wards, male and female medical wards.
  • was on at least one medication prior to admission
  • spoke Arabic or English and can be (the patient or care giver) interviewed for medication history
  • stayed in the hospital for at least 24 hours
  • discharged on at least one chronic medication or is at least on one chronic medication even if not prescribed upon discharge

Exclusion criteria

  • could not be interviewed due to language barrier, impaired cognition or other reasons and did not have a care giver
  • was under specialties other than medical specialties, but was admitted to medical wards because of lack of beds in their respective wards
  • was pregnant
  • was already included in the study at a previous admission
  • left the hospital against medical advice
  • with length of stay of >60 days.

Treatment and study plan

medication reconciliation intervention

Other

medication reconciliation intervention comprises medication reconciliation on admission and discharge, bedside medication counseling and take-home medication list

Primary outcomes

  1. number of patients with a preventable adverse drug event

    Time frame: 30 days

  2. number of potential adverse drug events

    Time frame: 30 days

Secondary outcomes

  1. number of emergency room visits

    Time frame: 30 days

  2. number of unplanned hospital visits

    Time frame: 30 days

  3. number of hospital readmissions

    Time frame: 30 days

  4. number of patients who traveled abroad to seek second medical opinion

    Time frame: 30 days

Sponsors and collaborators

Lead sponsor

Sultan Qaboos University

Other

Registry information

Official study title

Implementation of a Medication Reconciliation Intervention and Its Impact on the Rate of ADEs and Healthcare Utilization 30 Days Following Discharge From the Hospital. A Randomized Controlled Trial.

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jun 17, 2016
Registry last updated
Jun 21, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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