Status:

COMPLETED

Using Propranolol in Traumatic Brain Injury to Reduce Sympathetic Storm Phenomenon

Lead Sponsor:

Ain Shams University

Conditions:

Traumatic Brain Injury

Eligibility:

All Genders

18-60 years

Phase:

PHASE4

Brief Summary

Traumatic Brain Injury (TBI) is one of the leading causes of death. Severe TBT is correlated with an exaggerated stress response due to plasma catecholamine levels known as sympathetic storming. It is...

Detailed Description

The sympathetic storming events can be triggered by suctioning, repositioning, or environmental stimuli. To differentiate sympathetic storming from similar conditions, symptoms and signs have to occur...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Patients with isolated blunt TBI
  • From 18 to 60 years old both sex
  • Not in need of mechanical ventilation
  • GCS on admission between 9 and 12
  • Rotterdam CT score from 2-4.
  • Normal Procalcitonin test to exclude infection.
  • Exclusion criteria:
  • Preexisting heart disease
  • Myocardial injury
  • Craniotomy
  • Preexisting cerebral dysfunction
  • Spinal cord injury
  • Diabetes mellitus
  • Severe liver or kidney disease
  • Patients with sepsis

Exclusion

    Key Trial Info

    Start Date :

    October 1 2016

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    August 1 2017

    Estimated Enrollment :

    60 Patients enrolled

    Trial Details

    Trial ID

    NCT03401515

    Start Date

    October 1 2016

    End Date

    August 1 2017

    Last Update

    January 17 2018

    Active Locations (0)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 0 (0 locations)

    No Results Found

    We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.