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

Primary Purpose

Brain Injuries, Craniocerebral Trauma

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Long-term mild hypothermia
Normothermia
Sponsored by
RenJi Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Injuries focused on measuring Traumatic brain injury

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Department of Neurosurgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Long-term mild hypothermia

Normothermia

Arm Description

Focused intervention

Standard management

Outcomes

Primary Outcome Measures

Neurological function
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.

Secondary Outcome Measures

Intracranial pressure (ICP) control
The effect of long-term hypothermia on ICP control will be determined.
Glasgow Coma Score (GCS)
The neurological function improvement during study intervention will be evaluated.
Length of ICU stay
The numbers of days in the ICU.
Length of hospital stay
The numbers of days in the hospital.
Frequency of complications
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
The proportion of death will be determined at 6 months post injury.

Full Information

First Posted
June 17, 2013
Last Updated
March 10, 2020
Sponsor
RenJi Hospital
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, Southern Medical University, The Affiliated Hospital of Medical College of Chinese People's Armed Police Forces, Xiangya Hospital of Central South University, Taizhou First People's Hospital, Tang-Du Hospital, Qilu Hospital of Shandong University, Chongqing Emergency Medical Center, Xuzhou Central Hospital, The Affiliated Hospital Of Southwest Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT01886222
Brief Title
Randomized Controlled Trial of Long-term Mild Hypothermia for Severe Traumatic Brain Injury
Acronym
LTH-Ⅰ
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
November 12, 2013 (Actual)
Primary Completion Date
June 30, 2019 (Actual)
Study Completion Date
June 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
RenJi Hospital
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, Southern Medical University, The Affiliated Hospital of Medical College of Chinese People's Armed Police Forces, Xiangya Hospital of Central South University, Taizhou First People's Hospital, Tang-Du Hospital, Qilu Hospital of Shandong University, Chongqing Emergency Medical Center, Xuzhou Central Hospital, The Affiliated Hospital Of Southwest Medical University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Injuries, Craniocerebral Trauma
Keywords
Traumatic brain injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
312 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Long-term mild hypothermia
Arm Type
Experimental
Arm Description
Focused intervention
Arm Title
Normothermia
Arm Type
Other
Arm Description
Standard management
Intervention Type
Other
Intervention Name(s)
Long-term mild hypothermia
Other Intervention Name(s)
Mild hypothermia therapy
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Normothermia
Intervention Description
Patients assigned to the normothermia group will be kept at 36-37℃.
Primary Outcome Measure Information:
Title
Neurological function
Description
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.
Time Frame
6 months post injury
Secondary Outcome Measure Information:
Title
Intracranial pressure (ICP) control
Description
The effect of long-term hypothermia on ICP control will be determined.
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
Title
Glasgow Coma Score (GCS)
Description
The neurological function improvement during study intervention will be evaluated.
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
Title
Length of ICU stay
Description
The numbers of days in the ICU.
Time Frame
6 months post injury
Title
Length of hospital stay
Description
The numbers of days in the hospital.
Time Frame
6 months post injury
Title
Frequency of complications
Description
Frequency of complications during the the study such as pneumonia, significant bleeding, liver and kidney function abnormality will be recorded and compared between groups.
Time Frame
6 months post injury
Title
Mortality rate
Description
The proportion of death will be determined at 6 months post injury.
Time Frame
6 months post injury

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiyao Jiang, MD, PhD
Organizational Affiliation
Department of Neurosurgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, China
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Neurosurgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200127
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
16306933
Citation
Jiang JY, Xu W, Li WP, Gao GY, Bao YH, Liang YM, Luo QZ. Effect of long-term mild hypothermia or short-term mild hypothermia on outcome of patients with severe traumatic brain injury. J Cereb Blood Flow Metab. 2006 Jun;26(6):771-6. doi: 10.1038/sj.jcbfm.9600253.
Results Reference
background
PubMed Identifier
25460339
Citation
Lei J, Gao G, Mao Q, Feng J, Wang L, You W, Jiang J; LTH-1 trial collaborators. Rationale, methodology, and implementation of a nationwide multicenter randomized controlled trial of long-term mild hypothermia for severe traumatic brain injury (the LTH-1 trial). Contemp Clin Trials. 2015 Jan;40:9-14. doi: 10.1016/j.cct.2014.11.008. Epub 2014 Nov 12.
Results Reference
background
PubMed Identifier
33681741
Citation
Hui J, Feng J, Tu Y, Zhang W, Zhong C, Liu M, Wang Y, Long L, Chen L, Liu J, Mou C, Qiu B, Huang X, Huang Q, Zhang N, Yang X, Yang C, Li L, Ma R, Wu X, Lei J, Jiang Y, Liu L, Gao G, Jiang J; LTH-1 Trial collaborators. Safety and efficacy of long-term mild hypothermia for severe traumatic brain injury with refractory intracranial hypertension (LTH-1): A multicenter randomized controlled trial. EClinicalMedicine. 2021 Jan 28;32:100732. doi: 10.1016/j.eclinm.2021.100732. eCollection 2021 Feb.
Results Reference
derived
Links:
URL
http://www.chinese-neurotrauma.com/
Description
Shanghai Institute of Head Trauma leads the research on neurotrauma nationally and has made a lot of effort in traumatic brain injury.
URL
http://www.renji.com
Description
Ren Ji Hospital is one of the top medical centers across China.
URL
http://www.neurotraumasociety.org/
Description
Prof. Jiang holds the title of Chairman of International Neurotrauma Society.

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Randomized Controlled Trial of Long-term Mild Hypothermia for Severe Traumatic Brain Injury

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