Trials / Unknown
UnknownNCT04212208
Pain Assessment in the Perioperative Area
Pain Assessment in the Perioperative Area During IV Cannulation Using a Combination of EMLA and Low-frequency USG Probe Versus a Combination of EMLA Cream and High-frequency Probe in Pediatric Cases- A Randomized Control Trial
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- Sponsor
- All India Institute of Medical Sciences, Rishikesh · Other Government
- Sex
- All
- Age
- 5 Years – 12 Years
- Healthy volunteers
- Not accepted
Summary
This study is mainly focusing on reducing the pain scores during IV cannulation in pediatric population in the preoperative period. Applying EMLA cream is a well-known fact world wide. we would like to study the effect of ultrasound waves in the penetration of the given drung into the skin so that we could achieve the effect of the drug quickly.
Detailed description
To assess the intensity of pain in children in the perioperative area during IV cannulation using a combination of EMLA cream and low-frequency USG probe. To assess the intensity of pain in children in the perioperative area during IV cannulation using a combination of EMLA cream and high-frequency USG probe and final comparison between these groups will assess the effect of ultrasound in the penetration of the drug into the skin.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | IV cannulation | IV cannulation in the preoperative period |
Timeline
- Start date
- 2019-02-01
- Primary completion
- 2019-12-26
- Completion
- 2020-01-01
- First posted
- 2019-12-26
- Last updated
- 2019-12-27
Locations
1 site across 1 country: India
Source: ClinicalTrials.gov record NCT04212208. Inclusion in this directory is not an endorsement.