A CLINICAL STUDY TO STUDY EFFECTS OF TWO DRUGS ORAL TRICHLOPHOS AND INTRANASAL MIDAZOLAM FOR SEDATION IN CHILDREN.
Not Applicable
- Registration Number
- CTRI/2017/08/009448
- Lead Sponsor
- AIR FORCE HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
FOR CHILDREN FROM 01 MONTH TO 06 YRS FOR PROCEDURAL SEDATIO
Exclusion Criteria
SEVERE URTI
SICK CHILDREN WITH HEMODYNAMIC COMPROMISE
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO STUDY EFFICACY OF SEDATION <br/ ><br>COMPLETION OF PROCEDURE <br/ ><br>REQUIREMENT OF ADDITIONAL OUTCOME <br/ ><br>ADVERSE EFFECTS IF ANYTimepoint: 1. prior to starting procedure <br/ ><br>2. completion of procedure <br/ ><br>3. 10 min after completion of procedure <br/ ><br>
- Secondary Outcome Measures
Name Time Method ADVERSE EVENTS SUCH AS RESPIRATORY DEPRESSIO, HYPOXEMIA.AND POST PROCEDURAL SEDATIONTimepoint: EVERY 10 MIN UPTO 30 MI