Determination of NSI Regarding Bloodborne Pathogens Among Healthcare Workers at Tertiary Care, DIK (NCT07055100) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Determination of NSI Regarding Bloodborne Pathogens Among Healthcare Workers at Tertiary Care, DIK
Pakistan280 participantsStarted 2025-03-17
Plain-language summary
Bloodborne pathogens (BBPs) are a significant occupational hazard for healthcare professionals, particularly those working in high-risk environments like emergency departments. This study aims to assess the prevalence of bloodborne pathogens, including Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), and Human Immunodeficiency Virus (HIV), among emergency department staff of District Head Quarter (DHQ) Hospital, Dera Ismail Khan.
Who can participate
Age range
18 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Healthcare workers (doctors, nurses, technologists, paramedics, and support staff) working in a tertiary care hospital in Dera Ismail Khan.
* Staff members who have occupational exposure to blood and other body fluids.
* Individuals willing to participate in the study and provide informed consent.
* Participants available during the data collection period and conveniently accessible.
Exclusion Criteria:
* Individuals not willing to participate in the study and provide informed consent.
* Participants and Staff members who have no exposure to blood and other body fluids.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.