- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07914543
Drug Utilization and Prescribing Practices in the ENT Outpatient Department
Drug Utilization Patterns and Evaluation of Prescribing Practices Using WHO Prescribing Indicators in the ENT Outpatient Department
This cross-sectional, observational study evaluates drug utilization patterns and prescribing practices in the ear, nose, and throat (ENT) outpatient department using World Health Organization (WHO) core prescribing indicators. The study aims to assess prescription quality, the average number of drugs per encounter, antibiotic overuse, generic prescribing rates, and adherence to essential medicines lists to promote rational drug use and identify potential polypharmacy trends.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Shams A Kadhim
- Phone Number: +9647738645300
- Email: 97shamsali@gmail.com
Study Locations
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Basra, Iraq
- Al-Mawanee Teaching Hospital
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Contact:
- Alhasan Al-mudafeer
- Phone Number: +9647801601693
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Basra Governorate
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Basra, Basra Governorate, Iraq
- Al-Mawanee Teaching Hospital
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Contact:
- AL-Hassan M Almudafeer
- Phone Number: +9647801601693
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
All patients of any age group attending the Ear, Nose, and Throat (ENT) outpatient department and receiving at least one medical prescription during the study period.
Description
Inclusion Criteria:
- Patients attending the ENT outpatient department during the study period.
- Patients receiving at least one prescription.
- Patients of all age groups.
Exclusion Criteria:
- Incomplete prescriptions.
- Inpatients (admitted patients).
Study Plan
How is the study designed?
Design Details
- Observational Models: OTHER
- Time Perspectives: CROSS_SECTIONAL
Cohorts and Interventions
Group / Cohort |
|---|
|
ENT Outpatient Prescriptions
Prescriptions issued to patients attending the ear, nose, and throat (ENT) outpatient department during the study period. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Average Number of Drugs Per Prescription
Time Frame: During the 4-6 month study period
|
Assessment of the average number of medications prescribed per patient encounter in the ENT outpatient department using WHO prescribing indicators. |
During the 4-6 month study period
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of Encounters with Antibiotics
Time Frame: During the 4-6 month study period
|
To calculate the percentage of patient encounters where at least one antibiotic is prescribed in the ENT outpatient department. |
During the 4-6 month study period
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Percentage of Drugs Prescribed by Generic Name
Time Frame: During the 4-6 month study period
|
To assess the extent of generic prescribing relative to total drugs prescribed in the ENT outpatient department. |
During the 4-6 month study period
|
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Adherence to Essential Medicines List
Time Frame: During the 4-6 month study period
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To evaluate whether the prescribed medications are selected from the official essential medicines list. |
During the 4-6 month study period
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Alhasan M Al-mudafeer, AlFayhaa General Hospital
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- ENTWHO-2026-01
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
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