MedPath

Double Blind Study of Hypertonic Saline vs Mannitol in the Management of Increased Intracranial Pressure (ICP).

Not Applicable
Withdrawn
Conditions
Elevated Intracranial Pressure
Interventions
Drug: hypertonic saline
Registration Number
NCT01108744
Lead Sponsor
Beth Israel Deaconess Medical Center
Brief Summary

The study goal is to compare the management of increased intra-cranial pressure (ICP) using 3% hypertonic saline vs. mannitol (given in same osmolar loads).

Primary hypothesis:

1. Hypertonic saline will be non-inferior to mannitol in decreasing elevated ICP.

Secondary hypotheses:

1. Hypertonic saline therapy will result with fewer complications than mannitol

2. ICP reduction duration will be longer using hypertonic saline when compared with mannitol

Detailed Description

There is growing evidence in the literature indicating that ICP and Cerebral Perfusion Pressure measurements may not be sufficient in the management of elevated ICP. Based on this evidence, monitoring of partial brain tissue oxygenation has gain acceptance among neurosurgeons and neurointensivists, and has become a standard of care monitor in some centers across the country. There is, however, insufficient information in the literature describing the effects of hyperosmolar medications on regional brain tissue oxygenation.

We intend to undertake this non-inferiority, prospective, randomized double-blind study to answer very important clinical questions not yet answered in the literature: Will hypertonic saline therapy, given at equiosmolar load, be non-inferior to mannitol in reducing elevated ICP?

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Age ≥ 18 years
  • elevated ICP requiring ICP monitoring
  • ICP ≥ 25 mmHg 5 min after ICP bolt or EVD placement
Exclusion Criteria
  • Requiring decompressive craniotomy or post decompressive craniotomy
  • Hyponatremia (sodium level < 125 mEq/L)
  • Hypernatremia (sodium > 155 mmol/L)
  • Serum osmolality ≤ 250 mOsm/kg
  • Serum osmolality ≥ 320 mOsm/kg
  • Physical exam compatible with brain death
  • Patients on hemodialysis with end-stage renal disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
hypertonic salinehypertonic saline3% hypertonic saline, dosed by ideal patient weight
MannitolMannitol20% mannitol, dosed by patient's ideal body weight
Primary Outcome Measures
NameTimeMethod
Percent reduction of ICP from baseline30 minutes from completion of medication administration
Secondary Outcome Measures
NameTimeMethod
Time from study drug administration completion to ICP < 25 mmHgFirst 72 hours
Cumulative duration of ICP below 25 mmHgFirst 72 hours
Cumulative duration of cerebral perfusion pressure (CPP) above 60 mmHgFirst 72 hours
Cumulative duration of regional oxygen partial pressure (pbtO2) > 20%two hours following each dose administration during the first 24 hours
Total dose of medications givenFirst 24 hours; also over 3 days
Frequency of treatment failureFirst 72 hours

Treatment failure defined as ICP \> 30 mmHg for \> 30 minutes

Frequency of rebound intracranial hypertensionFirst 72 hours

Rebound intracranial hypertension defined as ICP \> 25 mmHg for more than 10 minutes following ICP stabilization

Frequency of composite Major Adverse Events3 days

1. acute kidney injury as defined by an increase in creatinine x 2 or GFR decrease \> 50% or urine output \< 0.5 ml/kg/h for 12 hours, compared to baseline, as per RIFLE criteria

2. hypotensive episodes (SBP \< 90 mmHg for more than 10 minutes)

3. hemodynamic instability as measured by decrease of cardiac output by more than 15% within two hours following medication administration

4. pulmonary edema as defined by ELWI I\> 10

Difference in inflammatory responseRegular intervals over first 3 days

Determined by analysis of cytokine and inflammatory biomarkers.

Difference in average pre-discharge stroke scale scorehospital discharge (or 30 days if not discharged)

Trial Locations

Locations (1)

Beth Israel Deaconess Medical Center

🇺🇸

Boston, Massachusetts, United States

© Copyright 2025. All Rights Reserved by MedPath