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Clinical Trials/CTRI/2023/02/050005
CTRI/2023/02/050005Completed未知

Comparison of changes in Analgesia Nociceptive Index, Surgical Pleth Index, andHemodynamic parameters to noxious stimuli in patients receiving opioid and opioid freeanalgesia undergoing supratentorial craniotomies – An open label comparative study.

ATIONAL INSTITUTE OF MENTAL HEALTH AND NEUROSCIENCES0 sites58 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
58

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • Patients aged between 18 and 65years of ASA I and II
  • -Patients undergoing elective supratentorial craniotomy

Exclusion Criteria

  • -Patients in whom dexmedetomidine is contraindicated (second and third degree heart block),
  • -Patients in whom ANI will be unreliable (patients with pacemakers, patients on drugs affecting
  • sinus node, patients having arrhythmias).
  • -Patients with liver and renal diseases.
  • -Patients on gabapentinoids, tricyclic antidepressants and other analgesics
  • -Patients posted for aneurysmal clipping
  • -Patients with decreased sensorium

Investigators

Sponsor
ATIONAL INSTITUTE OF MENTAL HEALTH AND NEUROSCIENCES

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