Medicines Reconciliation at an Intensive Care Unit

NCT ID: NCT03173690

Last Updated: 2017-07-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-06

Study Completion Date

2017-10-31

Brief Summary

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This study evaluates the effect of performing medicines reconciliation on patients admitted to an intensive care unit. Half of the patients will receive a medicines reconciliation at the intensive care unit. The other half will not. All included patients will receive medicines reconciliation after transfer to the ward.

Detailed Description

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Transfer of patients from one level of care to another is known to increase the risk of medication errors. Medication reconciliation is an accepted intervention to increase the knowledge on the patients medication use, thus reducing the risk of avoidable medication errors. For patients in the intensive care unit treatment of the imminent threat is obviously the most important. Nevertheless, knowledge about previous medications are important.

Conditions

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Medicines Reconciliation Intensive Care Unit

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The included patients are randomized to either intervention or control group. The intervention group receives medicines reconciliation at the intensive care unit. The control group receive standard pharmaceutical care, which now does not include medicines reconciliation. After the patients are transferred to care at the ward, medicines reconciliation is performed for all patients.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Caregivers
The care provider performing medicines reconciliation at ward is semimasked. The masking might be broken if the patients tells if he/she has been interviewed earlier in the study

Study Groups

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Intervention group

Receive medication reconciliation at the ICU, pluss medication reconciliation at the ward

Group Type EXPERIMENTAL

Medication reconciliation at the ICU

Intervention Type OTHER

Medication reconciliation performed according to Integrated Medicines Management model

Medication Reconciliation at the Ward

Intervention Type OTHER

Medication reconciliation performed according to Integrated Medicines Management model

Control group

No intervention at the ICU, medication reconciliation at the ward

Group Type OTHER

Medication Reconciliation at the Ward

Intervention Type OTHER

Medication reconciliation performed according to Integrated Medicines Management model

Interventions

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Medication reconciliation at the ICU

Medication reconciliation performed according to Integrated Medicines Management model

Intervention Type OTHER

Medication Reconciliation at the Ward

Medication reconciliation performed according to Integrated Medicines Management model

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* belonging to the hospitals intake area
* written informed concent by the patient or his/her next to kin

Exclusion Criteria

* Patients without next to kin
* Not Norwegian speaking, in need of a translator
* medication reconciliation performed earlier
* Patients with Guillain-Barre or Myasthenia Gravis, due to long expectancy of stay
* Short life expectancy, decided in cooperation with the physician
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospital Pharmacy Enterprise, South Eastern Norway

OTHER

Sponsor Role collaborator

University Hospital, Akershus

OTHER

Sponsor Role lead

Responsible Party

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Silje Engdal Ørnes

Clinical pharmacist, Ph.d

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Silje E Oernes, PhD

Role: PRINCIPAL_INVESTIGATOR

Hospital Pharmacy Enterprise, South Eastern Norway

Locations

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Akershus university Hospital

Lørenskog, Akershus, Norway

Site Status RECRUITING

Countries

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Norway

Central Contacts

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Silje E Oernes, phD

Role: CONTACT

004767960302

Facility Contacts

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Per Martin Baadstolokken

Role: primary

Other Identifiers

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16-186

Identifier Type: -

Identifier Source: org_study_id

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