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Randomized Controlled Trial of Long-term Mild Hypothermia for Severe Traumatic Brain Injury (LTH-Ⅰ)

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ClinicalTrials.gov Identifier: NCT01886222
Recruitment Status : Recruiting
First Posted : June 25, 2013
Last Update Posted : October 31, 2017
Sponsor:
Collaborators:
First Affiliated Hospital of Zhejiang University
West China Hospital
Second Affiliated Hospital of Wenzhou Medical University
The 101st Hospital of Chinese People's Liberation Army
The 98 Hospital of People's Liberation Army
Shenzhen Second People's Hospital
The 94 Hospital of People's Liberation Army
Nanfang Hospital of Southern Medical University
The Affiliated Hospital of Medical College of Chinese People's Armed Police Forces
Xiangya Hospital of Central South University
The First People's Hospital of Taizhou, Zhejiang
Tang-Du Hospital
Qilu Hospital of Shandong University
Chongqing Emergency Medical Center
Information provided by (Responsible Party):
Jiyao Jiang, RenJi Hospital

June 17, 2013
June 25, 2013
October 31, 2017
July 2013
June 2018   (Final data collection date for primary outcome measure)
Neurological function [ Time Frame: 6 months post injury ]
The neurological function will be evaluated at 6 months post injury by a specialized investigator who is 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.
Same as current
Complete list of historical versions of study NCT01886222 on ClinicalTrials.gov Archive Site
  • Intracranial pressure (ICP) control [ Time Frame: Admission, day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 14, or until the monitor is removed ]
    The effect of long-term hypothermia on ICP control will be determined.
  • Glasgow Coma Score (GCS) [ Time Frame: Admission, day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 14, day 21, day 28 post injury ]
    The neurological function improvement during study intervention will be evaluated.
  • Length of ICU stay [ Time Frame: 6 months post injury ]
    The numbers of days in the ICU.
  • Length of hospital stay [ Time Frame: 6 months post injury ]
    The numbers of days in the hospital.
  • Frequency of complications [ Time Frame: 6 months post injury ]
    Frequency of complications during the the study such as pneumonia, significant bleeding, liver and kidney function abnormality will be recorded and compared between groups.
  • Mortality rate [ Time Frame: 6 months post injury ]
    The proportion of death will be determined at 6 months post injury.
  • Intracranial pressure (ICP) control [ Time Frame: Admission, day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 14, or until the monitor is removed ]
    The effect of long-term hypothermia on ICP control will be determined.
  • Glasgow Coma Score (GCS) [ Time Frame: Admission, day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 14, day 21, day 28 post injury ]
    The neurological function improvement during study intervention will be evaluated.
  • Length of ICU stay [ Time Frame: 6 months post injury ]
    The numbers of days in the ICU.
  • Length of hospital stay [ Time Frame: 6 months post injury ]
    The numbers of days in the hospital.
  • Frequency of complications [ Time Frame: 6 months post injury ]
    Frequency of complications during the the study such as pneumonia, significant bleeding, liver and kidney function abnormality will be recorded and compared between groups.
Not Provided
Not Provided
 
Randomized Controlled Trial of Long-term Mild Hypothermia for Severe Traumatic Brain Injury
A Multi-center, Randomized, Controlled Trial to Evaluate the Efficacy and Safety of Long-term Mild Hypothermia in Adult Patients With Severe Traumatic Brain Injury

This study is a prospective multi-centre randomized trial to compare the effect of long-term mild hypothermia versus routine normothermic intensive management in patients with severe traumatic brain injury.

The primary hypothesis is that the induction of mild hypothermia (maintained at 34-35℃) for 5 days will improve the outcome of patients at six months post injury compared with normothermia.

Traumatic brain injury (TBI) remains a leading cause of death and disability in people with injuries and constitutes a major public health concern both in developed and developing countries. There are multiple clinical trials of hypothermia therapy for TBI conducted, however, with conflicting results. Subgroup analysis of most meta-analysis showed that therapeutic effect was significant when hypothermia was maintained more than 48 hours. We have previously reported a multicenter trial of mild hypothermia (33-35℃) for severe traumatic brain injury, in which 215 patients was randomized to long-term mild hypothermia group (n = 108) for 5 ±1.3 days mild hypothermia therapy and short-term mild hypothermia group ( n = 107) for 2±0.6 days mild hypothermia therapy. The results shown improved outcomes in patients with long-term mild hypothermia and similar frequency of complications. Therefore we concluded that long-term hypothermia, which maintains at 33-35℃ for 5 days, could be considered in the management of severe traumatic brain injury.

Hypothermia therapy was recommend as the level III evidence by the 2007 Brain Trauma Foundation's guideline and this treatment is currently used in our department and other large neurosurgical centers across China, with the aim to decrease the high intracranial pressure (ICP) and improve the functional outcome of TBI patients. When the decision was made, the injured patients would be placed on cooling blankets, tracheotomized and ventilated. The patients would receive continuous infusions of a paralytic drug (Tracrium 10-40 mg/hour) and chlorpromazine (5-10 mg/hour) administered using an infusion pump to prevent shivering. The dosage was given according to each patient's temperature, blood pressure, heart rate, and muscular tone. Once the patient's rectal temperature reached 33˚C, it was kept at approximately that temperature (33-35˚C) 5 to 7 days. Then the patients were passively rewarmed to a temperature of 37 to 38˚C at a rate no greater than 1˚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 (5 days) mild hypothermia versus normothermia on the outcome of patients following severe traumatic brain injury. The primary outcome is the neurological function assessed at 1, 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), need of surgery, 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.

Interventional
Not Applicable
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Brain Injuries
  • Craniocerebral Trauma
  • Other: Long-term mild hypothermia
    Hypothermia will be induced within 6 hours of injury and maintained at 34-35℃ for 5 days.Then the patients will be passively rewarmed to a temperature of 36 to 37˚C at a rate no greater than 0.5˚C/4 hours.
    Other Name: Mild hypothermia therapy
  • Other: Normothermia
    Patients assigned to the normothermia group will be kept at 36-37℃.
  • Experimental: Long-term mild hypothermia
    Focused intervention
    Intervention: Other: Long-term mild hypothermia
  • Normothermia
    Standard management
    Intervention: Other: Normothermia

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
300
240
December 2018
June 2018   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Age 18 - 65 years within 6 hours post injury;
  • Closed head injury;
  • Glasgow Coma Scale(GCS) score 4 to 8 after resuscitation;
  • The intracranial pressure is more than 25 mmHg;
  • Cerebral contusion on computed tomographic scan.

Exclusion Criteria:

  • GCS of 3 with bilateral fixed and dilated pupils;
  • A life-threatening injury to an organ other than the brain;
  • No spontaneous breathing or cardiac arrest at the scene of the injury;
  • No consent;
  • Pregnancy.
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult, Older Adult)
No
Contact: Guoyi Gao, MD, PhD 86-21-68383707 guoyigao@gmail.com
China
 
 
NCT01886222
RJNS001
Yes
Not Provided
Not Provided
Jiyao Jiang, RenJi Hospital
RenJi Hospital
  • First Affiliated Hospital of Zhejiang University
  • West China Hospital
  • Second Affiliated Hospital of Wenzhou Medical University
  • The 101st Hospital of Chinese People's Liberation Army
  • The 98 Hospital of People's Liberation Army
  • Shenzhen Second People's Hospital
  • The 94 Hospital of People's Liberation Army
  • Nanfang Hospital of Southern Medical University
  • The Affiliated Hospital of Medical College of Chinese People's Armed Police Forces
  • Xiangya Hospital of Central South University
  • The First People's Hospital of Taizhou, Zhejiang
  • Tang-Du Hospital
  • Qilu Hospital of Shandong University
  • Chongqing Emergency Medical Center
Principal Investigator: Jiyao Jiang, MD, PhD Department of Neurosurgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, China
RenJi Hospital
October 2017

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