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Sponsored by: |
Aarhus University Hospital |
Information provided by: | University of Aarhus |
ClinicalTrials.gov Identifier: | NCT00738816 |
Elderly patients has a higher risk of experiencing adverse drug events due to an age related increase in morbidity and medication use. Inappropriate or wrong medication use among elderly patients acutely admitted to hospitals is assumed to prolong patients inhospital stay if not corrected at admission to hospital. It is therefore our hypothesis that a systematic medication review conducted by pharmacists and physicians specialized in pharmacology will decrease elderly patients admission time in Orthopedic Departments from an average of five days to four days. Further, the following secondary outcome parameters will be measured at 3 and 12 month follow up:
Condition | Intervention |
Elderly |
Other: Systematic medication review and advisory notes |
Study Type: | Interventional |
Study Design: | Prevention, Randomized, Open Label, Uncontrolled, Parallel Assignment, Safety Study |
Official Title: | The Effect of Systematic Medication Review in Elderly Patients Admitted to an Orthopedic Department. |
Estimated Enrollment: | 100 |
Study Start Date: | September 2008 |
Estimated Study Completion Date: | October 2009 |
Estimated Primary Completion Date: | February 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
Intervention
Systematic medication review
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Other: Systematic medication review and advisory notes
Within 24 hours of admission a pharmacist retrieve medication histories from patients included in the intervention group. Medication histories will be obtained from - medical records, medication charts, patients electronical medication profile, interview with patients and if necessary contact to the patients general practitioner. The obtained medication history will be discussed with a physician specialized in pharmacology and an advisory note with suggested changes to the patients medication is added to the medical record. The orthopedic physicians are not obliged to follow the suggested changes
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Ages Eligible for Study: | 70 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Marianne Lisby, MHSc | +45 61264949 | lisby@as.aaa.dk |
Denmark, Central Denmark Region | |||||
Regional hospital, Randers | Not yet recruiting | ||||
Randers, Central Denmark Region, Denmark, 8900 | |||||
Contact: Lars Peter Nielsen, MD +45 89421987 lpn@dadlnet.dk | |||||
Principal Investigator: Marianne Lisby, MHSc |
Aarhus University Hospital |
Responsible Party: | Aarhus University Hospital ( Marianne Lisby ) |
Study ID Numbers: | Klinfarm |
First Received: | August 20, 2008 |
Last Updated: | August 20, 2008 |
ClinicalTrials.gov Identifier: | NCT00738816 |
Health Authority: | Denmark: Danish Dataprotection Agency; Denmark: The Danish National Committee on Biomedical Research Ethics |
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