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A clinical trial to study the effects of two anaesthetic drugs, Sevoflurane and desflurane in children undergoing short surgical procedures.

Phase 4
Completed
Conditions
Health Condition 1: null- Maintenance, Emergence and Recovery from General Anaesthesia in childrenPost operative agitation in children
Registration Number
CTRI/2015/02/005570
Lead Sponsor
okmanya Tilak Municipal Medical College and General Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

•Patients with history of sleep apnoea, developmental delay or psychological disorders.

•Patients with reactive airway disease or respiratory tract infections.

•Patient with significant pulmonary, cardiovascular, central nervous system, liver or kidney disease.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Emergence,Maintenance and Recovery CharacteristicsTimepoint: 1.Haemodynamic monitoring: every 2 minutes till the induction of anaesthesia and every 5 minutes till the end of surgery. <br/ ><br>2. Intra/post-operative adverse events <br/ ><br>3.Duration of anaesthesia <br/ ><br>4.Duration of surgery <br/ ><br>5.Duration of exposure to inhalational agents <br/ ><br>6.Time of discontinuation of anaesthesia <br/ ><br>7.Time to first cough <br/ ><br>8.Time to regular breathing <br/ ><br>9.Time to awakening <br/ ><br>10.Time of arrival to PACU <br/ ><br>11.Postoperative Agitation <br/ ><br>12.Post operative pain <br/ ><br>13.Post anaesthesia Recovery
Secondary Outcome Measures
NameTimeMethod
1. Haemodynamic alterations (Heart rate, Systollic & Diastolic Blood pressure) <br/ ><br>2.Assessment for pain (FLACC score) <br/ ><br>3.Intra-operative/post-operative adverse events like coughing, laryngospasm, bronchospasm, vomiting, etc <br/ ><br>Timepoint: -
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