Hypertonic Saline vs. Mannitol for Elevated Intercranial Pressure

This study has been terminated.
(A significant reduction in head injuries coupled with more frequent use of crainectomy reduced the number of potential subjects.)
Sponsor:
Collaborator:
Information provided by (Responsible Party):
University of Cincinnati
ClinicalTrials.gov Identifier:
NCT01111682
First received: April 22, 2010
Last updated: March 4, 2013
Last verified: March 2013

April 22, 2010
March 4, 2013
April 2010
November 2010   (final data collection date for primary outcome measure)
Proportion of time during which ICP is less than or equal to 20 mmHg during the first 120 hours following initiation of ICP monitoring. In the case where a patient is weaned from infusion, full ICP control will be assumed. [ Time Frame: 120 hours post initiation of monitoring ] [ Designated as safety issue: No ]
ICP will be recorded continuously and the proportion of time during which ICP is uncontrolled will be calculated. Specifically, this will be measured as any period during which ICP > 20 mmHg for 600 seconds or longer.
Same as current
Complete list of historical versions of study NCT01111682 on ClinicalTrials.gov Archive Site
  • Therapy Intensity Level (TIL), reflecting the amount and duration of therapy required to control ICP. TIL incorporates, among others, variables such as degree of head elevation, level of sedation, volume of CSF drainage, and hypocapnia. [ Time Frame: Daily ] [ Designated as safety issue: No ]
  • Long-term outcomes measured by Disability Rating Scale and Glasgow Outcome Scale-Extended [ Time Frame: 3 and 6 months post-injury ] [ Designated as safety issue: Yes ]
  • Incidence of pre-determined severe adverse events (SAEs): brain hypoxia, delayed decompression, pulmonary edema, renal failure, respiratory complications, seizures, systemic hypoxia, and uncontrollable ICP [ Time Frame: Each occurence of an SAE during the patient's hospital stay will be recorded. ] [ Designated as safety issue: Yes ]
    For each patient, we will count the number of SAEs in each category. Total SAEs by category and average number of SAEs per patient will be compared between the two study treatments.
Same as current
Not Provided
Not Provided
 
Hypertonic Saline vs. Mannitol for Elevated Intercranial Pressure
Hypertonic Saline vs. Mannitol for Elevated Intercranial Pressure

This study examines the role of osmotic agents in controlling brain swelling in brain injured individuals. Two osmotic agents -- mannitol and hypertonic saline -- are in common use, and they will be compared in the context of a randomized clinical trial. The goal is to determine if these agent differ in their ability to control episodes of brain swelling.

This single-center, randomized, open label trial will compare (i) 0.9% normal saline infusion and boluses of mannitol (control group) with (ii) 3% hypertonic saline, with intermittent boluses as needed, to treat elevated intracranial pressure (ICP) following severe traumatic brain injury.

Patients will be randomized to one of the two study arms following placement of an ICP monitor. Raised ICP will be defined as an ICP greater than 20 mmHG for 20 minutes or longer. In the event of such an event, the appropriate treatment will be administered.

The primary endpoint will be success in ICP control, operationalized as the proportion of time during which ICP is less than or equal to 20 mmHg during the first 120 hours following initiation of monitoring. Secondary endpoints include therapy intensity level, incidence of pre-determined severe adverse events, and long-term outcomes measured at 3 and 6 months post-injury.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Traumatic Brain Injury
  • Elevated Intracranial Pressure
  • Drug: Mannitol
    0.9% normal saline infusion and boluses of mannitol
  • Drug: Hypertonic Saline
    3% hypertonic saline continuous infusion, with intermittent boluses as needed
  • Active Comparator: Mannitol
    0.9% normal saline infusion and boluses of mannitol
    Intervention: Drug: Mannitol
  • Active Comparator: Hypertonic Saline
    3% hypertonic saline continuous infusion, with intermittent boluses as needed
    Intervention: Drug: Hypertonic Saline

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
5
November 2010
November 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • closed traumatic brain injury
  • either (i) GCS score 3-8 (inclusive), or (ii) GCS motor score of 5 or less AND abnormal admission CT scan showing intracranial pathology
  • hemodynamically stable with systolic blood pressure greater than 90 mmHg
  • at least 1 reactive pupil
  • age between 18y and 70y (inclusive)
  • INR less than 1.5

Exclusion Criteria:

  • actively on hypertonic saline or mannitol
  • hypernatremia (>145 meq/L)
  • anuric or with creatinine greater than or equal to 2.5
  • known seizure disorder
  • penetrating head trauma
  • suspected anoxic events
  • history of, or CT confirmation of, previous brain injury
  • any injury that, in the opinion of the Principal Investigator, has a high likelihood of death with the first 72 hours post-injury
  • any treatment, condition, or injury that contraindicates treatment with hypertonic saline
Both
18 Years to 70 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01111682
Shutter-2010-01
No
University of Cincinnati
University of Cincinnati
Department of Defense
Principal Investigator: Lori Shutter, MD Department of Neurology College of Medicine University of Cincinnati
University of Cincinnati
March 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP