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Needlestick InjuriesNCT07143422

Sharp Risks in a Time of Crisis: Needle-Stick Injuries in Eastern Sudan Healthcare

An observational study of Needlestick Injuries, run by National Center for Gastroentestinal and Liver Disease.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Background: Needle-stick injuries (NSIs) expose healthcare providers to serious bloodborne infections such as HBV, HCV, and HIV. These injuries are prevalent in Africa and worsened by poor training, limited resources, and systemic issues. Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Needlestick Injuries
How many people
272 participants
Where
No sites listed yet
Study dates
11 Sep 2015to 11 Sep 2017
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study population consists of doctors and nurses actively employed in healthcare facilities, including hospitals and clinics, within Kassala and Al Qadarif states in Eastern Sudan. These healthcare providers are at risk of needle-stick injuries due to their direct involvement in clinical procedures using needles and sharps. Non-clinical staff, hygienists, medical students, and other personnel not directly involved in patient care or exposure to sharps were excluded. A census with stratified random sampling was used to ensure proportional representation across professions and healthcare settings.

Who may be able to join

  • Doctors who are currently employed and actively working in healthcare facilities such as hospitals and clinics in Kassala and Al Qadarif states, Eastern Sudan.
  • Nurses who are currently employed and actively working in healthcare facilities such as hospitals and clinics in Kassala and Al Qadarif states, Eastern Sudan.
  • Healthcare providers who are at risk of needle-stick injuries as part of their routine clinical duties, including procedures involving needles and sharps.
  • Participants who provide informed consent to take part in the study.

Who cannot join

  • Non-clinical staff who do not engage in direct patient care or handling of needles and sharps, such as administrative personnel.
  • Hygienists and other support staff whose job roles do not involve exposure to needle-stick injuries.
  • Medical students and trainees who are not fully employed healthcare providers within the facilities at the time of the study.
  • Individuals who do not consent or refuse to participate in the study.

About this study

Official title: Sharp Risks in a Time of Crisis: A Study of Needle-Stick Injuries in Eastern Sudan's Healthcare Sector - A Cross-Sectional Study

Background: Needle-stick injuries (NSIs) expose healthcare providers to serious bloodborne infections such as HBV, HCV, and HIV. These injuries are prevalent in Africa and worsened by poor training, limited resources, and systemic issues. In Sudan, the ongoing war has intensified healthcare challenges, increasing NSI risks.

Methods: A cross-sectional survey was conducted among doctors and nurses in Eastern Sudan using an interview-based questionnaire. Stratified random sampling ensured proportional representation. Data were analyzed using SPSS (p < 0.05). Ethical approval and informed consent were obtained.

Keywords
Needlestick injuries, Health care workers, Safety
Medical subject headings
Needlestick Injuries

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prevalence of Needle-Stick Injuries Among Healthcare Workers

    Percentage of healthcare workers reporting ≥1 needle-stick injury.

    Measured: 6 months

Secondary outcomes (1)
  1. Proportion of healthcare workers reporting needle-stick injury reporting behavior

    Percentage of participants who reported their needle-stick injuries to hospital authorities or occupational health services, assessed by questionnaire.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Aug 2025
  2. Study start11 Sep 2015
  3. Primary completion15 Nov 2016
  4. Study completion11 Sep 2017

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
272 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07143422
Sponsor's protocol ID
ncgld
Status last verified
Aug 2025
First submitted
8 Aug 2025
Last updated
27 Aug 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Needlestick Injuries, run by National Center for Gastroentestinal and Liver Disease.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prevalence of Needle-Stick Injuries Among Healthcare Workers (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Aug 2025.

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