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Clinical Trials/CTRI/2018/05/013682
CTRI/2018/05/013682
Completed
未知

To evaluate the dose requirement of propofol for induction of anaesthesia in patients with traumatic brain injury using bilateral Bispectral Index

ational Institute of Mental Health And Neurosciences0 sites96 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- Patients with traumatic brain injury coming for surgeryHealth Condition 2: S065- Traumatic subdural hemorrhage
Sponsor
ational Institute of Mental Health And Neurosciences
Enrollment
96
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
May 11, 2018
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
ational Institute of Mental Health And Neurosciences

Eligibility Criteria

Inclusion Criteria

  • Patients of either sex, aged between 18\- 60 years with mild, moderate and severe traumatic brain injury (TBI) presenting for surgery within 48 hours of trauma .

Exclusion Criteria

  • Patients who are hemodynamically unstable, patients with relative refusing to give consent, patients in whom BIS recording is not possible, patients with anticipated difficult airway, patients history of severe cardiac, pulmonary, liver or renal disease, or obesity (body mass index \>30\) and pregnancy.

Outcomes

Primary Outcomes

Not specified

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