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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03442608
Other study ID # LTHSAH-1
Secondary ID
Status Not yet recruiting
Phase N/A
First received January 16, 2018
Last updated February 23, 2018
Start date March 1, 2018
Est. completion date December 31, 2020

Study information

Verified date February 2018
Source Xuanwu Hospital, Beijing
Contact Xin Qu, MD,PhD
Phone 86-10-83198633
Email xinqu0213@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date December 31, 2020
Est. primary completion date December 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Procedure:
Zoll 2000 and/or CureWrap 3500 cooling system
Device(Zoll 2000 and/or CureWrap 3500 cooling system),lasting 5 to 7 days, the core temperature will be controlled in 33-35 degree.

Locations

Country Name City State
n/a

Sponsors (14)

Lead Sponsor Collaborator
Xuanwu Hospital, Beijing Beijing Tiantan Hospital, Central South University, First Affiliated Hospital of Fujian Medical University, First Affiliated Hospital of Harbin Medical University, First Affiliated Hospital of Wenzhou Medical Univeristy, First Hospital of Jilin University, Qilu Hospital of Shandong University, Second Affiliated Hospital, School of Medicine, Zhejiang University, Shandong Provincial Hospital, Shanxi Province Cardiovascular Hospital, Tang-Du Hospital, The First Affiliated Hospital of Dalian Medical University, Yantai Yuhuangding Hospital

References & Publications (1)

Seule MA, Muroi C, Mink S, Yonekawa Y, Keller E. Therapeutic hypothermia in patients with aneurysmal subarachnoid hemorrhage, refractory intracranial hypertension, or cerebral vasospasm. Neurosurgery. 2009 Jan;64(1):86-92; discussion 92-3. doi: 10.1227/01.NEU.0000336312.32773.A0. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Neurological function 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. 6 months after hemorrhage
Secondary Intracranial pressure 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, until the monitor is removed
Secondary Length of ICU stay The numbers of days in the ICU 6 months post hemorrhage
Secondary Length of hospital stay The numbers of days in the hospital. 6 months post hemorrhage
Secondary Frequency of complications 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. 6 months post hemorrhage
Secondary Mortality rate The proportion of death will be determined 6 months after hemorrhage
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