- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05898282
Prevalence and Associated Factors of Anesthetic Drug Administration Error, a Web Based Crossectional Survey, 2022.
Prevalence and Associated Factors of Anesthetic Drug Administration Error Among Anesthetists Working in Teaching and Referral Hospitals of Ethiopia, a Web Based Crossectional Survey, 2022.
The operating room (OR) is a demanding and time-constrained setting, in comparison to primary care settings, where perioperative medication administration is more complicated and there is a high risk that the patient will experience a medication error.
Without consulting the pharmacist or seeking assistance from other staff members, anesthesia clinicians prepare, deliver, and monitor strong anesthetic drugs.
Study Overview
Status
Intervention / Treatment
Detailed Description
The operating room (OR) is a demanding and time-constrained setting, in comparison to primary care settings, where perioperative medication administration is more complicated and there is a high risk that the patient will experience a medication error. Anesthesia clinicians prepare, deliver, and monitor strong anesthetic drugs without consulting pharmacists or seeking assistance from other staff members.
The aim of this study was to determine the prevalence of medication administration errors by anesthetists and associated factors in referral and teaching hospitals in the Amhara region of, Ethiopia.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Debre Tabor, Ethiopia, 271
- Debre Tabor University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- all anesthetists with a minimum of six months of working experience, the ability to respond to the questionnaire using the listed online choices, and involvement in direct patient care to be included in the study.
Exclusion Criteria:
- Anesthetists who were not involved in medication administration and those serving in administrative positions were excluded from the study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
anesthesia professionals
anesthetists working at teaching and referral hospitals of north west Ethiopia
|
since this is a cross sectional observational study any form of intervention was not applicable
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of anesthetics drug administration error by anesthetists working in Amhara region, Ethiopia
Time Frame: October 1-November 30, 2022
|
This study aimed to determine the type, frequency, and factors that lead to medication errors in patients under anesthesia. This study aimed to determine the type, frequency, and factors that lead to medication errors in patients under anesthesia. This study aimed to determine the type, frequency, and factors that lead to medication errors in patients under anesthesia |
October 1-November 30, 2022
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
factors associated with medication administration errors by anesthetists
Time Frame: October 1-November 30, 2022
|
This study aimed to determine the type, frequency, and factors that lead to medication errors in patients under anesthesia
|
October 1-November 30, 2022
|
Collaborators and Investigators
Sponsor
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
Keywords
Other Study ID Numbers
- DebreTaborU
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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