Clinical trial to compare sedation and analgesia rotation and non rotation protocol in mechanically ventilated childre
Not Applicable
- Conditions
- Health Condition 1: Z991- Dependence on respirator
- Registration Number
- CTRI/2023/02/049865
- Lead Sponsor
- Aiims jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Children between one month to 18 years whose anticipated duration of requiring sedation and analgesia is for more than 3 days (72 hours).
2. Parents or guardians giving informed written consent for enrollment of child into study.
Exclusion Criteria
Patients in whom drug rotation may not be possible as they would be requiring deeper sedation like in pulmonary hypertension.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the occurrence of withdrawal symptoms in sedation drug rotation protocol versus sedation with no rotation using WAT-1 (withdrawal assessment tool version 1). <br/ ><br>Timepoint: After 1 year (March 2024) <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.To compare the cumulative dose of midazolam needed as rescue therapy in both groups. <br/ ><br>2.To compare the total duration of mechanical ventilation in each group. <br/ ><br>3.To compare the total duration of PICU stay in each group.Timepoint: Till 1 year (March 2024)