IRCT20230714058776N1
Completed
N/A
The Effect of ShotBlocker in Reducing Pain Associated with Peripheral Intravenous Cannulation in School Age Children: A Randomized Controlled Trial (RCT)
College of Nursing, University of Baghdad0 sites128 target enrollmentTBD
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Pain management related intravenous cannulation.
- Sponsor
- College of Nursing, University of Baghdad
- Enrollment
- 128
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Consent to volunteer to participate in the study.
- •Being between the ages of 6 and 12 years.
- •Intravenous cannulation will be applied in right and left hand only.
- •No difficulty in communication, including hearing, visual, speech, and language problems.
- •Not receiving oral or parenteral analgesic treatment before administration.
- •Not receiving chemotherapy treatment.
Exclusion Criteria
- •Skin conditions such as burns, rashes, open wounds, abscess or boil, severe local infection or cellulitis at the intended insertion site.
- •Peripheral vascular disease or compromised peripheral circulation at the intended insertion site (e. g. Peripheral neuropathy, diabetes, Peripheral artery disease, Raynaud's disease).
- •Blood clotting disorders or increased risk of bleeding (e.g., hemophilia, thrombocytopenia).
- •Anatomical abnormalities or restrictions that impede proper insertion or cause increased risk of complications.
- •History of injections during the last 3 months.
Outcomes
Primary Outcomes
Not specified
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