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A study to assess confusion and restlessness after general anaesthesia with sevoflurane in adults.

Evaluation of incidence of sevoflurane induced emergence delirium following general anaesthesia in adults- An observational study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/01/100314
Enrollment
80
Registered
2026-01-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: F40-F48- Anxiety, dissociative, stress-related, somatoform and other nonpsychotic mental disorders

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: SEVOFLURANE: No comparator agent (single arm observational study)

Sponsors

CHETTINAD HOSPITAL AND RESEARCH INSTITUTE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Posted for general anesthesia 2.Only elective cases 3.Duration of surgery more than 2hours.

Exclusion criteria

Exclusion criteria: 1.Patients known to have preexisting diseases such as history of chronic dementia psychosis mental retardation cerebrovascular accidents with residual cognitive impairment. 2.Neurological surgeries 3.Psychiatric conditions 4.Pregnancy 5.Emergency surgery 6.Patients with BMI more than 35 7.Patient refusal.

Design outcomes

Primary

MeasureTime frame
To determine incidence of emergence delirium with sevoflurane in adults.Timepoint: 150 mins—

Secondary

MeasureTime frame
To identify factors associated with emergence delirium with sevoflurane in adults in perioperative period following general anesthesiaTimepoint: 150mins—

Countries

India

Contacts

Public ContactDR VIJAY NARAYANAN S

CHETTINAD HOSPITAL AND RESEARCH INSTITUTE

vijaynarayanans@care.edu.in7904535573

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026