About this trial
The goal of this observational study is to develop and implement Medication errors reporting system using the error reporting guidelines. The main question it aims to answer is:
"Does development and implementation of Medication errors reporting guideline will help to reduce the errors rate and improve the patient safety?"
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
For the quantitative part, the inclusion criteria are patients of all age groups and prescriptions issued to inpatients.
For the qualitative part of the study, inclusion criteria are healthcare professionals aged more than 18 years working in Dhulikhel Hospital.
Disqualifiers
The exclusion criteria will be incomplete and unclear prescriptions.
The healthcare persons who accepted the consent but couldn't complete the survey will be excluded from the study.
Trial population
Healthcare professionals including Doctors, Nurses and Pharmacist who are working in Dhulikhel Hospital.
Trial design
Other
Cross-sectional
Treatments tested in this trial
medication errors reporting guidelines
Other interventionthe intervention is designed to reduce the medication errors and develop the culture of reporting the Medication errors in clinical settings.
Treatment groups
Trial outcomes
Primary outcomes
reduction in Mediation error rate
The newly developed Medication errors reporting guidelines will be implemented and will be used to evaluate the reduction in medication errors incident rates.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: