pain intensity in children at the time of intravenous catheter inseration.
Conditions
Interventions
Intervention 1: Intervention group: The cold spray used in this study includes a cold spray product from Italy, with the exclusive representation of the medical equipment company of modern medicine. I
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
6 Years to 12 Years
Inclusion criteria
Inclusion criteria: Age 6 to 12 years No need for branol insertion in vital cases, such as cardiopulmonary resuscitation or seizure ... Do not use of systemic or topical analgesics based on taking a biographical report of the child and parents within 24 hours before inserting branol Absence of neurological defects such as (organ neuropathy, paralysis of the limbs) affecting perception of pain based on the biography of the child, the parents and the clinical examination No history of allergies, skin dermatitis and ulcers in the target area (such as the back of the arm) for insertion of a venous catheter Insensitivity to cold
Exclusion criteria
Exclusion criteria: Lack of proper cooperation from the child and the child's parents Failure to install branol in the first attempt Not having enough time to do the basics before installing branol in emergency situations
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Intensity. Timepoint: During the arrival of the Branol. Method of measurement: Wang Baker smileys. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactArash Khalili
Hamedan University of Medical Sciences
Outcome results
None listed