Skip to main content
OpenTrials
Completed

NCT Number: NCT00178659

Proteomics of Brain Trauma-associated Elevated Intracranial Pressure (ICP)

The specific aim of this research is to determine if the blood from brain-injured patients contains reproducible protein markers that appear prior to elevations in intracranial pressure (ICP).

Completed

Looking for future studies?

Notify Me

Key information

Age range

14 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The University of Texas, Houston

Houston, Texas, 77030, United States

About this study

One of the major causes of death following brain trauma is increased intracranial pressure (ICP). Currently, there are no effective ways to predict if the ICP of a patient will reach uncontrollable levels. Various cytokines (balance between pro-and anti-inflammatory) and other factors are thought to underlie increases in ICP. The specific aim of this research is to determine if the blood from brain-injured patients contains reproducible protein markers that appear prior to elevations in ICP. We propose to employ mass spectrometry, antibody array and ELISA to profile proteins in the serum of patients suffering from traumatic brain injury. These protein profiles will be compiled by a pattern recognition program that has the capacity to learn and make predictions based on the spectra and associated patient information. Each time a sample is analyzed, it is added to the database allowing the program to make increasingly accurate predictions. Protein profiles of patients with known ICP values will be analyzed. Our hypothesis is that alterations in serum protein composition will precede changes in intracranial pressure giving rise to predictable patterns that can be detected using large-scale proteomic analysis. After approximately 90 non-brain trauma and 90 brain-trauma patients are analyzed, if markers are found, the predictability of elevated ICP will be tested. If successful, this may aid the neurosurgeon in determining future courses of treatment.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 14-65 years old
  • Non-penetrating brain injury
  • ICP monitor or
  • Healthy volunteer or

The orthopedic injury cohort will include patients admitted to the ED able to provide informed consent with the following:

  • Fracture confirmed radiographically
  • No head trauma
  • No other known inflammatory process or infection
  • No history of neurological or psychiatric disorders or alcohol or drug dependency.

or The mild TBI patients will be defined as those experiencing,

  • Non-penetrating head trauma manifesting one or more of the following:
  • Loss of consciousness
  • Post-traumatic amnesia
  • Altered mental status
  • Focal neurologic deficits, seizure
  • GCS> 12
  • No abnormalities on CT other than contusion
  • No operative Lesions
  • Length of hospital stay < 48 hrs
  • No other known inflammatory process or infection
  • No history of neurological or psychiatric disorders or alcohol or drug dependency

Exclusion criteria

  • Inability to obtain informed consent

Treatment and study plan

Blood/saliva samples for protein/molecular analysis

Other

Bloods samples - healthy volunteers(1 time) head injury subjects (5 times). Blood and/or saliva samples mild TBI patients (2 times) and healthy volunteers (2 times)

Other names: blood samples, saliva samples

Primary outcomes

  1. Elevated intracranial pressure

    Time frame: within the first 10 days post injury

    Intracranial pressure >20mmHg

Sponsors and collaborators

Lead sponsor

The University of Texas Health Science Center, Houston

Other

Collaborators

  • TIRR/Mission Connect
  • The Center for Clinical and Translational Sciences (CCTS) Clinical Research Unit at The University of Texas Health Science Center at Houston

Registry information

Acronym: Proteomics

Important dates

Study start
2004
Primary completion
2015
Study completion
2026
First posted
Sep 15, 2005
Registry last updated
Jun 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.