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NCT06428162 Clinical Trial

An Evaluation of Healthcare Providers' Adherence to Pharmacovigilance Practices in an African Community

Drug Abuse Clinical Trial

Official title:
an Observational Study for the Prevalence of Pharmacovigilance Practices Between Healthcare Providers in North African Nation

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT06428162
Other study ID # 2024 PV
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date February 18, 2024
Est. completion date June 20, 2024

Study information
Verified date June 2024
Source Deraya University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Egypt's several regions-rural, mixed, and urban-were given pre-designed surveys pertaining to drug adverse events and the role of pharmacovigilance in detection and reporting. The three sections of the survey were dedicated to studying health care professionals' knowledge concerning pharmacovigilance concepts and practices, as well as demographics and people reported or not reported. The survey also asked more questions regarding adverse occurrences that were reported.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 300
Est. completion date June 20, 2024
Est. primary completion date May 20, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 55 Years
Eligibility Inclusion Criteria: - all health care providers are invited to share in the study - minimum experience required is one year in health carrier. - accept sharing in the study Exclusion Criteria: - health care providers who refuse to complete all data required in the survey. - fresh experience or participants who left health carrier

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• questionner
three sections questioner including: demographics, reported cases, unreported cases

Locations
Country Name City State
Egypt Deraya university Minya

Sponsors (1)
Lead Sponsor Collaborator
Deraya University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary reported adverse drug reactions collect recent adverse drug reaction reports 3 months
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