Cerebral Hemodynamic Effects of Hypertonic Solutions in Severely Head-Injured Patients

Sponsor
The University of Texas Health Science Center at San Antonio (Other)
Overall Status
Terminated
CT.gov ID
NCT00125229
Collaborator
(none)
10
1
10
1

Study Details

Study Description

Brief Summary

This is a clinical study comparing the physiologic effects of two hypertonic solutions (mannitol, hypertonic saline) with a particular emphasis on changes in cerebral blood flow in patients with intracranial hypertension following serious traumatic brain injury (TBI).

Condition or Disease Intervention/Treatment Phase

Detailed Description

This is a study comparing effects of two hypertonic solutions (mannitol, 6.4% hypertonic saline) on intracranial hypertension, cerebral blood flow, serum/urine osmolarity in patients with increased intracranial pressure caused by traumatic brain injury. The study is conducted during first 72 hours after the injury without any interference with standard medical treatment as performed at the institution. When the hypertonic solution is indicated by caregiver, the study team is informed and performs a set of physiologic bedside measurements including evaluation of cerebral blood flow and changes in plasma and urine osmolarity. The study is noninvasive and the study protocol does not hamper, in any way, standard care of treatment for these patients.

Study Design

Study Type:
Observational
Anticipated Enrollment :
10 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Cerebral Hemodynamic Effects of Hypertonic Solutions in Severely Head-Injured Patients
Study Start Date :
Aug 1, 2005
Actual Primary Completion Date :
Jun 1, 2006
Actual Study Completion Date :
Jun 1, 2006

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with severe TBI (motor Glasgow Coma Scale [GCS] score < 5)

    • Age > 18 years

    • Health care provider indicated a treatment of intracranial hypertension using hyperosmotic agent

    Exclusion Criteria:
    • Brain dead (GCS 3, fixed dilated pupils)

    • Life-threatening systemic injuries (AIS > 4 in an organ system other than brain); AIS = Abbreviated Injury Score

    • Hypotension not responsive to fluid resuscitation and low doses of dopamine

    • Clinical or imaging sign/suspicion for internal carotid artery injury

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Center for Neurosurgery Sciences - UTHSCSA - Surgical Intensive Care Unit (SICU) San Antonio Texas United States 78229

    Sponsors and Collaborators

    • The University of Texas Health Science Center at San Antonio

    Investigators

    • Principal Investigator: Roman Hlatky, M.D., Center for Neurosurgical Sciences - UTHSC San Antonio

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    The University of Texas Health Science Center at San Antonio
    ClinicalTrials.gov Identifier:
    NCT00125229
    Other Study ID Numbers:
    • 045-1503-266
    First Posted:
    Jul 29, 2005
    Last Update Posted:
    Jun 26, 2012
    Last Verified:
    Jun 1, 2012
    Keywords provided by The University of Texas Health Science Center at San Antonio
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 26, 2012