Assessment of injection pain due to an intravenous anaesthetic agent propofol in children.
Phase 4
- Conditions
- Health Condition 1: null- pediatric patients age group - 6 months to 8 yearsASA grade I and II
- Registration Number
- CTRI/2017/06/008850
- Lead Sponsor
- okmanya Tilak Municipal Medical College and general hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 170
Inclusion Criteria
ASA GRADE I and II patients
Exclusion Criteria
1)Patients with known allergy to eggs.
2)Patients with bradycardia.
3)Patients with hypotension.
4)Patients still crying/not calmed down, even after 5 minutes of sedation.
5)Parents not willing to give consent for study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method a.Incidence of pain following propofol injection <br/ ><br>b.Severity of pain <br/ ><br>Timepoint: Following propofol injection <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method Hemodynamic parametersTimepoint: 1) Before sedation <br/ ><br>2) After sedation <br/ ><br>3) After propofol injection