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Trial of Long-term Therapeutic Hypothermia for Poor-grade Aneurysmal Subarachnoid Hemorrhage

Not Applicable
Conditions
Hypothermia
Aneurysmal Subarachnoid Hemorrhage
Interventions
Procedure: Zoll 2000 and/or CureWrap 3500 cooling system
Registration Number
NCT03442608
Lead Sponsor
Xuanwu Hospital, Beijing
Brief Summary

This study is a prospective, multi-centre, randomized,controlled trial to compare the efficacy of long-term mild hypothermia with normothermic intensive management in patients with poor-grade aneurysmal subarachnoid hemorrhage.

The primary hypothesis is that the induction of mild hypothermia (maintained at 32-35℃) for at least 5 days would improve the outcome of patients at six months post hemorrhage compared with normothermia.

Detailed Description

Aneurysmal subarachnoid hemorrhage (aSAH), especially poor-grade aSAH, is a medical emergency with very high morbidity and mortality rates. SAH constitutes a major public health concern in developed and developing countries. There were several clinical trials of hypothermia for aSAH conducted, however, with conflicting results.

Hypothermia therapy treatment is currently used in our department and other large neurosurgical centers across China to decrease the intracranial pressure (ICP), mitigate some of the destructive processes, and improve the functional outcome of patients with poor-grade aSAH. When the decision was made, the patients would be placed in wrapped cooling blankets or intravascular cooling device after they were sedated, intubated and mechanically ventilated. The patients would receive continuous infusions of some drugs using an infusion pump to prevent shivering. Once the patient's rectal, nasopharyngeal or blood temperature reached 32˚C, it was kept at approximately that temperature (32-35˚C) 3 to 7 days. Then the patients were passively rewarmed to a temperature of 36 to 37˚C at a rate no greater than 0.25˚C/hour, by gradual adjustment of the blanket thermostat.

The present multi-center, randomized controlled trials is designed to investigate the efficacy and safety of long-term (3 days) mild hypothermia versus normothermia on the outcome of patients with poor-grade aSAH. The primary outcome is the neurological function assessed at 1,3, 6 months post injury with the Glasgow Outcome Score (GOS). Additionally, the following data will also be recorded and compared: the baseline data, Glasgow Coma Score,imaging examination (e.g. CT scan), intracranial pressure, laboratory tests (e.g. blood routine test, liver and kidney function, blood gas analysis, etc), the complications (e.g. pneumonia, significant bleeding) and so on.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Age 18 - 65 years within 72 hours after subarachnoid hemorrhage;
  • Neurosurgical clipping or coiling for aneurysm;
  • Hunt-Hess IV-V scale;
  • The intracranial pressure is more than 20 mmHg.
Exclusion Criteria
  • GCS of 3 with bilateral fixed and dilated pupils;
  • No spontaneous breathing or cardiac arrest at the scene of hemorrhage;
  • No consent;
  • Pregnancy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
mild hypothermiaZoll 2000 and/or CureWrap 3500 cooling systemDevice: Zoll 2000 and/or CureWrap 3500 cooling system,lasting 5 to 7 days, the core temperature will be controlled in 33-35 degree.
northermiaZoll 2000 and/or CureWrap 3500 cooling systemnormal physical cooling methods,like ice bag, conditionally required.
Primary Outcome Measures
NameTimeMethod
Neurological function6 months after hemorrhage

The neurological function will be evaluated at 6 months after hemorrhage by 2 specialized investigators who are unaware of the patients' allocation according to five-category Glasgow Outcome Scale as follows: 1, death; 2, vegetative state - unable to interact with the environment; 3, severe disability - unable to live independently but able to follow commands; 4, moderate disability - capable of living independently but unable to return to work or school; and 5, good recovery - able to return to work or school.

Secondary Outcome Measures
NameTimeMethod
Intracranial pressureAdmission, day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 14, until the monitor is removed

The effect of long-term hypothermia on ICP control will be determined.

Length of ICU stay6 months post hemorrhage

The numbers of days in the ICU

Length of hospital stay6 months post hemorrhage

The numbers of days in the hospital.

Frequency of complications6 months post hemorrhage

Frequency of complications during the the study such as pneumonia, coagulation disturbance,electrolyte disturbances, liver and kidney function abnormality will be recorded and compared between groups.

Mortality rate6 months after hemorrhage

The proportion of death will be determined

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