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Perioperative respiratory adverse events during deep verses awake extubation in pediatric population

Periperative respiratory adverse events during deep versus awake extubation in pediatric patients - a single centered prospective randomized control trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073235
Enrollment
218
Registered
2024-09-02
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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: Extubation: Extubation done either in deep or awake plane of anesthesia. Intervention2: Deep Extubation: Deep Extubation in pediatric operation theatre study participants during the stu

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Asa 1 and 2 patients posted for elective abdominal and urological procedures of less than 4 hours duration.

Exclusion criteria

Exclusion criteria: Children less than 60 weeks post conceptional age, reactive airway disease, full stomach and high risk of aspiration, severe OSA, BMI more than 95 or less than 5th centile, craniofacial anomaly, any trauma or difficult airway, hemodynamic or metabolic abnormality.

Design outcomes

Primary

MeasureTime frame
Major airway complications at emergence that will be recorded are desaturation, laryngospasm, bronchospasm, regurgitation, stridor, persistent coughing, negative pressure pulmonary edema.Timepoint: 1 year

Secondary

MeasureTime frame
Incidence of minor airway complications like cough, breath holding, increased airway secretions, tube biting and minor airway obstruction. Other parameters are hemodynamic variations, emergence delerium, need of oxygen and airway support in PACU,need for admission in ICUTimepoint: 1 year

Countries

India

Contacts

Public ContactAnu K A

Seth GSMC and KEM Hospital

anukaaluva@gmail.com08450970818

Outcome results

None listed

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