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Clinical Trials/CTRI/2013/05/003605
CTRI/2013/05/003605CompletedPhase 3

Entropy monitoring for titrating target controlled infusion(TCI)requirements of propofol in adults undergoing laryngeal surgery under total intravenous anaesthesia(TIVA)with or without supplementary dexmedetomidine infusion

Anjolie Chhabra0 sites50 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor
Enrollment
50

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • •This study will be conducted in the Department of Anaesthesiology at All India Institute of Medical Sciences after obtaining Institutional Ethics committee approval. 60 ASA I and II patients, 18-65 years, undergoing laryngotracheal procedures requiring suspension laryngoscopy, rigid bronchoscopy will be included in this study after taking informed consent

Exclusion Criteria

  • •1.Patients who have neurological deficit following head injury, epilepsy etc. which can interfere with entropy monitoring.
  • •2. Patients who are morbidly obese (BMI >35kg/m2).
  • •3. Patients on β blockers, clonidine, verapamil.

Investigators

Sponsor
Anjolie Chhabra

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