- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05832788
Occupational Hazards and Associated Health Effects Among Workers in Main Assiut University Printing Press
Study Overview
Status
Conditions
Detailed Description
Printing in its simplest forms has existed for thousands of years, in the form of signet rings, royal seals and punches used by gold and silver-smiths.
Each printing process is divided into 3 major steps: prepress, press, and post-press. Prepress operations include the composition, typesetting, graphic arts photography, assembly of images and preparation of image carrier. Press includes the actual printing operation. Post-press involves the assembly of printed materials, binding and finishing operations.
Workers in printing press are exposed to, chemical, physical, ergonomic, and psychological hazards.
Chemical hazards are the most serious one. due to exposure to lot of chemical substances such as organic solvents, inks, adhesives, organic and inorganic pigments, The most important chemical substances used are Volatile Organic compounds, and inks.
Exposure to these chemicals occurs through both inhalation and dermal contact, The Acute symptoms include dizziness, drowsiness, eye irritation,.etc. Long-term health effects may include damage of internal organs as liver, kidneys and lungs, brain, reproductive system, bladder etc.
Dermatitis is a common health effect among printing workers due to exposure to chemicals.
One of the intended components of inks, solvents, and cleaning agents form is Benzene, long term exposure to benzene cause blood disorders. It specifically affects bone marrow, thus leading to decrease in the erythrocytes and leukocytes production resulting in anemia, myeloid leukemia, thrombocytopenia.
Noise is health hazard to which those workers are exposed, it occurs during printing, binding, folding.
Ergonomic hazards are hazards among those workers in the form of serious accidents and musculoskeletal disorders.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Fatma EL Zahraa Mohamed
- Phone Number: 01023638562
- Email: fatmaelzahraam734@aun.edu.eg
Study Contact Backup
- Name: Shimaa Abd El Samee
- Phone Number: 01000525137
- Email: shima_dola@yahoo.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 1. Workers with more than one year work duration.
- 2. both sexes, males and females.
Exclusion Criteria:
- 1. Workers who have any blood health problems as blood cells disorders and bleeding disorders before they started working.
2. Pre-employment liver diseases and kidney diseases among those workers. 3. Workers with less than one year work duration.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
• Describe the occupational hazards and associated negative health effects of these hazards among workers at Main Assiut University Printing Press.
Time Frame: 3 years
|
• Laboratory investigations and questionnaire will be used to assess this measure
|
3 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
• Identify associated risk factors to these effects among the study workers.
Time Frame: 3 years
|
• questionnaire will be used to assess this measure
|
3 years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Other Study ID Numbers
- printing hazards
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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