Evaluation of the effect of painless spray in reducing local pai
Phase 3
Recruiting
- Conditions
- Procedural pain.
- Registration Number
- IRCT20180129038549N13
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
All adult patients referred to the emergency department of al-Zahra and Kashani hospitals Need for Central Venous Catheter Insertion
Alert
Stable vital signs
Exclusion Criteria
The presence of visual, mental and verbal disorders
Sensitivity to anesthetic drugs
Sensory or motor disorder of the upper extremities
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The severity of pain. Timepoint: After intravenous cannulation. Method of measurement: Numeric Analogue Scale (NAS).
- Secondary Outcome Measures
Name Time Method Drug side effects such as redness, whitening and skin blemishes. Timepoint: Until the time of discharge. Method of measurement: Standard questionnaire form.