- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03182972
Intervention Study on Medication Reconciliation Among Pharmacists in Two Tertiary Hospitals in Nigeria
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background information garnering will be done among the pharmacists in the two selected hospitals to collect data on current practice of medication reconciliation. Focus group discussion will be done in the intervention group so as to identify peculiarities of their practice and to provide the best approach to carrying out the intervention. Diabetes and hypertensive patients in medical outpatient clinic will be interviewed in order to assess current practice of medication reconciliation.
Intervention will be channeled towards addressing gaps discovered. University College Hospital, Ibadan, Oyo State will be the intervention group, while University of Ilorin Teaching Hospital, Kwara State will be the control group.
The effect of the intervention will be measured over time to ensure that medication reconciliation is implemented in the selected institutions.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kwara
-
Ilorin, Kwara, Nigeria
- University of Ilorin Teaching Hospital
-
-
Oyo
-
Ibadan, Oyo, Nigeria, 2334
- University College Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participant has diabetes and/or hypertension
- Registered pharmacists in the selected institutions
Exclusion Criteria:
- Participants that are neither diabetic nor hypertensive
- Unregistered pharmacists in the selected institutions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention arm
Seminar presentation will be done using the followings:
|
Pre-post intervention
|
No Intervention: Control arm
Control group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Medication reconciliation: Percentage unreconciled medications
Time Frame: 3 months
|
Percentage unreconciled medications
|
3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: TITILAYO O FAKEYE, PhD, University of Ibadan
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MR/UCH/FMC/73247
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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