- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04588584
Prescribing Practice of Medication - Patient View.
October 8, 2020 updated by: Medical University of Graz
Prescribing Practice of Medicinal Products From the Perspective of the Patient.
In the clinical routine of a hospital, there are often problems dealing with medication that has already been prescribed at the time of admission due to incomplete or missing medication lists from the family doctor. Often patients forget this list at home.
This pilot study focuses on the medication process from admission to discharge and patient health literacy.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Styria
-
Graz, Styria, Austria, 8036
- LKH University clinical Graz , QM-RM
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
100 patients in the primary care clinic
Description
Inclusion Criteria:
- Patient hospitalised at the clinical ward of Endocrinilogy and Diabetology and plastic Surgery
- Patient with an minimum of 2 days hospitalisation
- good knowledge of German
- Age 18 to 99 Years
- Male/female
Exclusion Criteria:
- Neurological or psychiatric primary disease e.g. Dementia
- Rehospitalisation 7 days after discharge from hospital
- Patients who need intensive care
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Health competence of patients with focus on drugs.
Time Frame: 6 months
|
Correct knowledge of the medication (indication) - assessed by Interview with the patient
|
6 months
|
Drug prescription from the view of the patient- Amount
Time Frame: 6 months
|
Amount of prescribed drugs by descriptive chart review with CRF (Case Report Form) and interview with the patient
|
6 months
|
Drug prescription from the view of the patient- Type of drugs
Time Frame: 6 months
|
Type of prescribed drugs by descriptive chart review with CRF and interview with the patient
|
6 months
|
Drug prescription from the view of the patient- Discrepancies
Time Frame: 6 months
|
Potential discrepancies between amount or type of drugs indicated by the patient and descriptive chart review with CRF
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 19, 2018
Primary Completion (Actual)
July 31, 2020
Study Completion (Actual)
September 30, 2020
Study Registration Dates
First Submitted
October 8, 2020
First Submitted That Met QC Criteria
October 8, 2020
First Posted (Actual)
October 19, 2020
Study Record Updates
Last Update Posted (Actual)
October 19, 2020
Last Update Submitted That Met QC Criteria
October 8, 2020
Last Verified
October 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- EK_NR_30-178 ex 17/18
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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