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SEVOFLURANE Vs PROPOFOL FOR ANAESTHESIA MAINTENANCE IN PAEDIATRIC MRI

COMPARISON OF SEVOFLURANE AND PROPOFOL FOR MAINTENANCE OF ANAESTHESIA IN PAEDIATRIC MRI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/12/029961
Enrollment
274
Registered
2020-12-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: G403- Generalized idiopathic epilepsy and epileptic syndromes

Interventions

Intervention1: Sevoflurane: In children who have been randomly assigned to receive sevoflurane (Group S), an appropriately sized facemask will be secured in place using a harness. The dial concentrati

Sponsors

Seth GS Medical College and KEM Hospital Mumbai
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiology (ASA) status I and II children between 1-12years of age, without any evidence of an anticipated difficult airway and severe systemic disease.

Exclusion criteria

Exclusion criteria: 1. Severe cardiovascular, pulmonary, endocrine, renal and hepatic disease 2. Severe airway or craniofacial abnormality 3. History of propofol intolerance, family history of malignant hyperthermia and mitochondrial disease, 4. Fat metabolism disorder 5. Imaging for acute trauma 6. History suggestive of recent respiratory tract infection 7. Inadequate fasting 8. Children receiving intravenous anesthetic agents or sedative agents other than propofol 9. Children with tracheostomy in-situ 10. Children requiring mechanical ventilation, supplemental oxygen and inotropic support

Design outcomes

Primary

MeasureTime frame
To estimate the efficacy of sevoflurane in comparison to propofol in terms of interruptions in paediatric MRI during maintenance of anaesthesiaTimepoint: On completion of the MRI scan

Secondary

MeasureTime frame
To compare the following parameters between the two study groups: (a) Time to awakening (b) Time spent in PACU until fulfillment of PACU discharge criteria (c) Incidence of respiratory complications during the MRI scan (d) Incidence of cardiovascular complications during the MRI scan (e) Incidence of emergence delirium (g) Incidence of post-procedure vomitingTimepoint: All the above mentioned secondary outcomes will be assessed on completion of MRI scan

Countries

India

Contacts

Public ContactAkhil Goel

Seth GS Medical College and KEM Hospital, Mumbai

akhilgoel.in@gmail.com9923686533

Outcome results

None listed

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