Brain Injuries Clinical Trial
— LTH-?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
NCT number | NCT01886222 |
Other study ID # | RJNS001 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 12, 2013 |
Est. completion date | June 30, 2019 |
Verified date | March 2020 |
Source | RenJi Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 312 |
Est. completion date | June 30, 2019 |
Est. primary completion date | June 30, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
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. |
Country | Name | City | State |
---|---|---|---|
China | Department of Neurosurgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University | Shanghai | Shanghai |
Lead Sponsor | Collaborator |
---|---|
RenJi Hospital | Chongqing Emergency Medical Center, First Affiliated Hospital of Zhejiang University, Nanfang Hospital of Southern Medical University, Qilu Hospital of Shandong University, Second Affiliated Hospital of Wenzhou Medical University, Shenzhen Second People's Hospital, Tang-Du Hospital, The 101st Hospital of Chinese People's Liberation Army, The 94 Hospital of People's Liberation Army, The 98 Hospital of People's Liberation Army, The Affiliated Hospital of Medical College of Chinese People's Armed Police Forces, The Affiliated Hospital Of Southwest Medical University, The First People's Hospital of Taizhou, Zhejiang, West China Hospital, Xiangya Hospital of Central South University, Xuzhou Central Hospital |
China,
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. — View 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. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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. | 6 months post injury | |
Secondary | Intracranial pressure (ICP) control | The effect of long-term hypothermia on ICP control will be determined. | Admission, day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 14, or until the monitor is removed | |
Secondary | Glasgow Coma Score (GCS) | The neurological function improvement during study intervention will be evaluated. | Admission, day 1, day 2, day 3, day 4, day 5, day 6, day 7, day 14, day 21, day 28 post injury | |
Secondary | Length of ICU stay | The numbers of days in the ICU. | 6 months post injury | |
Secondary | Length of hospital stay | The numbers of days in the hospital. | 6 months post injury | |
Secondary | 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. | 6 months post injury | |
Secondary | Mortality rate | The proportion of death will be determined at 6 months post injury. | 6 months post injury |
Status | Clinical Trial | Phase | |
---|---|---|---|
Enrolling by invitation |
NCT05542108 -
Adding Motion to Contact: A New Model for Low-cost Family Centered Very-early Onset Intervention in Very Preterm-born Infants
|
N/A | |
Completed |
NCT03400904 -
Extubation Strategies in Neuro-Intensive Care Unit Patients and Associations With Outcome.
|
||
Completed |
NCT06073145 -
Transcranial Doppler Using Wearable Ultrasound Patch
|
||
Recruiting |
NCT03899532 -
Remote Ischemic Conditioning in Traumatic Brain Injury
|
N/A | |
Recruiting |
NCT06010823 -
Safety and Efficacy Evaluation of the Robotic Enhanced Error Training of Upper Limb Function in Post-stroke and Post TBI Participants
|
N/A | |
Not yet recruiting |
NCT05833568 -
Five-day 20-minute 10-Hz tACS in Patients With a Disorder of Consciousness
|
N/A | |
Withdrawn |
NCT04288076 -
The Brain and Lung Interaction (BALI) Study
|
N/A | |
Completed |
NCT03162484 -
Physical Activity and Chronic Acquired Brain Injury
|
N/A | |
Not yet recruiting |
NCT02756585 -
Computed Tomography Perfusion in Patients With Severe Head Injury
|
N/A | |
Terminated |
NCT01430988 -
Observational Study of the BrainScope® Ahead™ M-100 in UK Emergency Department Patients With Head Injury
|
N/A | |
Completed |
NCT01093053 -
Mind-Body Skills Groups for the Treatment of War Zone Stress in Military and Veteran Populations
|
N/A | |
Completed |
NCT00975338 -
The LETS Study: A Longitudinal Evaluation of Transition Services
|
||
Completed |
NCT00878631 -
Feasibility Trial of Traumatic Brain Injured Patients Randomized in the Prehospital Setting to Either Hypertonic Saline and Dextran Versus Normal Saline
|
Phase 2/Phase 3 | |
Completed |
NCT03166722 -
Cerebral Regional Tissue Oxygen Saturation to Guide Oxygen Delivery in Preterm Neonates During Immediate Transition
|
N/A | |
Not yet recruiting |
NCT04478812 -
Tbit System Precision and Correlation of Different Blood Samples
|
N/A | |
Recruiting |
NCT05443542 -
VIrtual Reality in Cognitive Rehabilitation of Processing Speed for Persons With ABI
|
N/A | |
Recruiting |
NCT05309005 -
Virtual Reality and Social Cognition After Acquired Brain Injury
|
||
Completed |
NCT02702635 -
Measuring Blood Flow Characteristics Using Dynamic Contrast Enhanced Magnetic Resonance Imaging
|
N/A | |
Withdrawn |
NCT04247321 -
Non-invasive Near-infrared Spectroscopy (NIRS) Versus Invasive Licox Intracranial Pressure
|
N/A | |
Not yet recruiting |
NCT04386525 -
Omega 3 and Ischemic Stroke; Fish Oil as an Option
|
Phase 4 |