- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01291251
Compliance With Antibiotic Treatment in General Practice
April 23, 2012 updated by: Torunn Bjerve Eide, Norwegian Medical Association
The guidelines of The Norwegian authorities concerning the use of antibiotics in general practice state that for several common diseases such as pneumonia and tonsillitis, antibiotics should be given four times daily instead of three times daily.
The study´s aim is to see whether the patient compliance is significantly reduced in antibiotic regimes of 3 or 4 daily doses as compared to 1 or 2 daily doses.
Study Overview
Status
Completed
Conditions
Detailed Description
All patients given antibiotic tablets, independent of diagnosis and medicament, are included.
All patients give a written consent.
Within a week after the end of the treatment all patients are contacted by one of the authors and asked a few standardized questions concerning their compliance with the treatment.
Study Type
Observational
Enrollment (Actual)
270
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
-
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Aust-Agder
-
Arendal, Aust-Agder, Norway, 4816
- Hisøy legekontor
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Froland, Aust-Agder, Norway, 4820
- Froland legekontor
-
-
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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients in two different primary care clinics.
Description
Inclusion Criteria:
- Any patient given antibiotics for any cause
Exclusion Criteria:
- Use of mixture instead of tablets
- Tablets administrated by public health care services
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
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Mette Brekke, Ph D, University of Oslo
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
February 1, 2010
Primary Completion (ACTUAL)
December 1, 2010
Study Completion (ACTUAL)
February 1, 2012
Study Registration Dates
First Submitted
February 7, 2011
First Submitted That Met QC Criteria
February 7, 2011
First Posted (ESTIMATE)
February 8, 2011
Study Record Updates
Last Update Posted (ESTIMATE)
April 24, 2012
Last Update Submitted That Met QC Criteria
April 23, 2012
Last Verified
April 1, 2012
More Information
Terms related to this study
Other Study ID Numbers
- VH-TBE-1
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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