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Clinical Trials/CTRI/2024/02/063090
CTRI/2024/02/063090
Not yet recruiting
未知

Quantitative Pupillometric evaluation to noxious stimulation for prognostication of patients with acute traumatic brain injury - A prospective observational study - NI

IMHANS0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: S064- Epidural hemorrhageHealth Condition 2: S063- Focal traumatic brain injuryHealth Condition 3: S020- Fracture of vault of skullHealth Condition 4: S018- Open wound of other parts of headHealth Condition 5: S068- Other specified intracranial injuriesHealth Condition 6: S066- Traumatic subarachnoid hemorrhageHealth Condition 7: S065- Traumatic subdural hemorrhage

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: S064- Epidural hemorrhageHealth Condition 2: S063- Focal traumatic brain injuryHealth Condition 3: S020- Fracture of vault of skullHealth Condition 4: S018- Open wound of other parts of headHealth Condition 5: S068- Other specified intracranial injuriesHealth Condition 6: S066- Traumatic subarachnoid hemorrhageHealth Condition 7: S065- Traumatic subdural hemorrhage
Sponsor
IMHANS
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational

Investigators

Sponsor
IMHANS

Eligibility Criteria

Inclusion Criteria

  • •All adult patients (18 \- 75 years of age), with moderate to severe TBI admitted to Neuro ICU/ward within 48 hours of injury

Exclusion Criteria

  • •1\. Absence of feasibility of performing Quantitative Pupillometry(QP) and ONSD assessment on the eye contralateral to the side with significant TBI (contralateral eye with pupillary disease or significant periorbital oedema where pupillary assessment is not possible)
  • •2\. Patients for whom consent is not available
  • •3\. Patients with significant co\-morbidities/ extra cranial injuries where these are likely to affect survival

Outcomes

Primary Outcomes

Not specified

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