Pharmacist Discharge Medication Reconciliation Study

Sponsor
Alberta Health services (Other)
Overall Status
Completed
CT.gov ID
NCT01226589
Collaborator
(none)
50
1
12
4.2

Study Details

Study Description

Brief Summary

Adverse drug events can occur commonly due to medication errors during the transition of care in a health care facility. Medication reconciliation is the process of comparing medications and providing an accurate medication list as a resource for prescribers, which is currently only being done upon inpatient admission at the CCI. The purpose of this study is to see if pharmacist medication reconciliation at discharge reduces unintentional medication discrepancies for inpatient discharges.

Condition or Disease Intervention/Treatment Phase
  • Procedure: MRS
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Impact of Pharmacist Discharge Medication Reconciliation on Unintentional Medication Discrepancies From Inpatient Discharges at the Alberta Cancer Board Cross Cancer Institute
Study Start Date :
Oct 1, 2007
Actual Study Completion Date :
Oct 1, 2008

Outcome Measures

Primary Outcome Measures

  1. MRS Correlation with Treatment Response. [up to 1 year]

    The percentage of patients with at least one unintentional medication discrepancy after discharge from the Cross Cancer Institute

Secondary Outcome Measures

  1. Correlation with Tumor Stage [up to 1 year]

    The amount of medication discrepancies after discharge that has the potential to cause moderate harm to severe harm.

  2. The frequency of each type of unintentional medication discrepancies. []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Cancer inpatients under the care of Dr. Follett or Dr. Candler

  • Cancer inpatients to be discharged from the CCI

  • Patients >18 years of age

  • Patients that are taking >1 medications or herbals total at home.

Exclusion Criteria:
  • Cancer inpatients that are considered radioactive or in "hot rooms" (ie. Selectron patients or patients receiving radiation treatment for thyroid)

  • Patients that do not remain in hospital >72 hours

  • Patients without a home phone number or equivalent contact number.

  • Language barrier (patients unable to speak or understand English).

  • Patients that are readmitted and already included into the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cross Cancer Institute Edmonton Alberta Canada T6G 1Z2

Sponsors and Collaborators

  • Alberta Health services

Investigators

  • Principal Investigator: Carole Chambers, BSc. Pharmacy, AHS Cancer Control Alberta

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01226589
Other Study ID Numbers:
  • 23851
First Posted:
Oct 22, 2010
Last Update Posted:
Apr 19, 2011
Last Verified:
Apr 1, 2011

Study Results

No Results Posted as of Apr 19, 2011