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Effect of 2 different doses of Dexmedetomidine to prevent adverse respiratory events in Paediatric population.

Comparison of two different dosages of premedication with dexmedetomidine to prevent adverse respiratory events after removal of supraglottic airway devices in paediatric patients.A prospective randomized study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074208
Enrollment
130
Registered
2024-09-24
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Comparison Of Two Different Dosages Of Dexmedetomidine In Paediatric age group.: The Two Different dosages Of Dexmedetomidine is used to prevent adverse respiratory events after removal

Sponsors

DR ANKITA ASHISH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Parenteral consent. 2.Patients of ASA grade 1&2. 3.Patients scheduled for surgeries of less than 2 hours

Exclusion criteria

Exclusion criteria: 1.History of congenital heart disease,neurological disease and asthma. 2.Patients with hiatal hernia,major abdominal or thoracic surgery. 3.Patients with full stomach. 4.Difficult airway or facial anomaly.

Design outcomes

Primary

MeasureTime frame
To see occurence of any one of respiratory events like coughing,bronchospasm,LMA biting.Timepoint: Baseline—

Secondary

MeasureTime frame
To see emergence agitation, postoperative nausea & vomiting.Timepoint: Baseline—

Countries

India

Contacts

Public ContactDR ANKITA ASHISH

Indira Gandhi Institute Of Medical Sciences

drhussain72@yahoo.co.in7004224089

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026