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Anaesthesia for MRI in childre

Phase 4
Conditions
Health Condition 1: null- Patients between the ages of 1 to 7 years requiring anaesthesia services for MRI studies
Registration Number
CTRI/2017/03/008008
Lead Sponsor
okmanya Tilak Municipal Medical College and General Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
70
Inclusion Criteria

ASA class I and II

Exclusion Criteria

1)ASA status: III and above

2)Severe cardiovascular or pulmonary pathology

3)History of Propofol allergy

4)Any contraindications for Dexmedetomidine administration

5)Anatomical craniofacial anomaly or suspected difficult airway

6)Evidence of raised intracranial pressure or active seizures.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1)To study the efficacy of total intravenous anesthesia which is defined by <br/ ><br>â?¢Sedation success rate <br/ ><br>â?¢Quality of scan as per the radiologist <br/ ><br>â?¢Recovery time <br/ ><br>â?¢Discharge time <br/ ><br>Timepoint: every 5 minutes during the procedure <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
To study the safety profile of total intravenous anesthesia, defined by the occurrence of <br/ ><br>â?¢Haemodynamic adverse events: <br/ ><br>Bradycardia <br/ ><br>Hypotension <br/ ><br>â?¢Respiratory adverse events: <br/ ><br>Bradypnoea (RR 12/min) <br/ ><br>Desaturation (SpO295%) <br/ ><br>Laryngospasm <br/ ><br>Apnoea (cessation of respiration for 20 s) <br/ ><br>Need of airway intervention measures (jaw thrust, Guedels or laryngeal mask airway, endotracheal tube, or positive pressure ventilation). <br/ ><br>â?¢Emergence reaction: determined by the Watcha scale on awakening. <br/ ><br>Timepoint: At the end of the procedure <br/ ><br>At the end of the recovery period
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