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Pharmacist Discharge Medication Reconciliation Study

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01226589
First Posted: October 22, 2010
Last Update Posted: April 19, 2011
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
AHS Cancer Control Alberta
  Purpose
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 Intervention
Medication Reconciliation Procedure: MRS

Study Type: Interventional
Study Design: 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

Further study details as provided by AHS Cancer Control Alberta:

Primary Outcome Measures:
  • MRS Correlation with Treatment Response. [ Time Frame: 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:
  • Correlation with Tumor Stage [ Time Frame: up to 1 year ]
    The amount of medication discrepancies after discharge that has the potential to cause moderate harm to severe harm.

  • The frequency of each type of unintentional medication discrepancies.

Estimated Enrollment: 50
Study Start Date: October 2007
Study Completion Date: October 2008
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01226589


Locations
Canada, Alberta
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
  More Information

Responsible Party: Carole Chambers, Alberta Cancer Board
ClinicalTrials.gov Identifier: NCT01226589     History of Changes
Other Study ID Numbers: 23851
First Submitted: October 21, 2010
First Posted: October 22, 2010
Last Update Posted: April 19, 2011
Last Verified: April 2011

Keywords provided by AHS Cancer Control Alberta:
Cancer cancer
MRS
Treatment response
Histologically confirmed diagnosed Breast cancer.
Patient is 18 years or older.
Karnofsky performance score is equal to or greater than 70.
No previously irradiated or recurrent breast.
No contraindication to MRS/MRI.