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Hypothermia clinical trials

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NCT ID: NCT00791050 Not yet recruiting - Anesthesia Clinical Trials

Examine the Effects of Maintaining Body Core Temperature During CABGs

Start date: January 2009
Phase: N/A
Study type: Interventional

Although data on cardioprotective effects (as profile of troponin I)of perioperative maintenance of normothermia during CABGs are already known, little is known about the effects of maintaining normothermia on clinical outcomes of patients submitted to coronary surgery. Being acute renal failure (ARF) and atrial fibrillation (AF) the two most frequent complications of this surgery, this study compare as primary end point the rate of postoperative ARF and AF in two group of patients, one actively warmed with Thermowrap and the control group receiving standard institutional care.

NCT ID: NCT00774631 Terminated - Clinical trials for Bacterial Meningitis

IHPOTOTAM : Induced HyPOthermia TO Treat Adult Meningitis

IHPOTOTAM
Start date: March 2009
Phase: Phase 4
Study type: Interventional

Bacterial meningitis is a severe infection of the envelope which surrounds the brain. It is sometimes responsible for a cerebral oedema mattering with a loss of consciousness (coma). The usual treatment of this affection is based on the antibiotic therapy, anti-inflammatory drug and resuscitation measures in intensive care setting but the prognosis of comatose patients remains poor. Moderate hypothermia (body temperature is downed between 32 and 34°C°) made the proof of its efficiency in certain cerebral pathologies (notably the cerebral distress after cardiac arrest or oxygen lack in neonates) but was never evaluated in meningitis. In meningitis animal studies and in severe traumatic brain injury, moderate hypothermia is able to diminish cerebral oedema and brain inflammation. Thus, the objective of this study is to compare two strategies: only usual care or usual care completed by moderate hypothermia. The body temperature will be lowered between 32 and 34°C by means of a catheter placed in a big vein and connected to a machine in which circulates a cold liquid, or by means of an external cooling (ice-cold blanket, ice packs placed on the body). Whatever technique is chosen, the technique is perfectly mastered by the teams which take charge of the patients. After 48 hours, the technique of hypothermia will be suspended and body temperature will return passively and gradually to normal. The investigators believe that moderate hypothermia will improve the prognosis of the most severe patients.

NCT ID: NCT00772460 Completed - Hypothermia Clinical Trials

Comparison of a New Patient Warming System Using Polymer Conductive Warming With Forced Air Warming During Surgery

HDV
Start date: October 2008
Phase: Phase 3
Study type: Interventional

Two patient warming systems will be compared with 40 patients each in a convective warming group (BairHugger, Arizant) and in a conductive warming group (HotDog, Augustine Biomedical). The patients will undergo small to medium trauma surgery and will be warmed with the randomized device - the hypothesis is, that the area under the standardized core temperature / time curve is significantly greater in the conductive warming group. Secondary outcome is the mean skin temperature / time area under the curve.

NCT ID: NCT00766103 Completed - Clinical trials for Cerebral Metabolism and Perfusion

The Effects of PaCO2 Levels on Cerebral Metabolism and Perfusion During Induced Hypothermia.

Start date: December 2006
Phase: N/A
Study type: Interventional

Incidence of hypo- and hypercarbia during induced hypothermia after cardiac arrest is high. The original report from HACA-group reported that hypothermia treated patients had improved survival and neurological outcome. Suprisingly, in that trial normocarbia was not achieved even though the aim was set for ventilatory support as normoventilation. This study aims to investigate the effects of mild hypo- and hypercarbia on cerebral perfusion (blood flow, intracranial pressure) and metabolism (microdialysate metabolites). We hypothesize that uncontrolled ventilatory suppport may render the patients in risk of exacerbation of neuronal damage, conversely, further improvement in outcome may be achieved with succesfull ventilatory management. We intend to enroll 10 out-of-hospital cardiac arrest patients succesfully resuscitated and subsequently treated with controlled hypothermia for 24 hours. The patients in need of anticoagulation are excluded. We plan to induce mild hypocarbia and hypercarbia during and after induced hypothermia. Metabolic and perfusion data are collected with clinically used methods such as transcranial doppler, intracranial pressure measurement, near infrared spectroscopy, jugular bulb, intracerebral microdialysis).

NCT ID: NCT00763828 Not yet recruiting - Clinical trials for ST-Elevation Myocardial Infarction

Can Hypothermia be Incorporated Into Primary Angioplasty for Heart Attack?

CHIPAHA
Start date: January 28, 2024
Phase: N/A
Study type: Interventional

The hypothesis of this study is that consciously sedated patients suffering from ST-elevation myocardial infarction can be rapidly and safely cooled to a state of therapeutic hypothermia (32 to 34 degrees C) using the LRS ThermoSuit System prior to percutaneous coronary intervention.

NCT ID: NCT00754481 Completed - Cardiac Arrest Clinical Trials

Hypothermia for Cardiac Arrest in Paediatrics

Start date: January 2005
Phase: Phase 2
Study type: Interventional

The investigators hypothesized that, following cardiac arrest in pediatric patients, hypothermia therapy will improve the proportion of patients with a good functional outcome compared to a normothermic control group.

NCT ID: NCT00712023 Completed - Hypothermia Clinical Trials

Effect of Forced-air Warming and Circulating-water Mattress in Preventing Heat Loss During Vascular Surgery

Start date: July 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether a custom-made forced-air warming mattress can prevent heat loss in patients undergoing vascular surgery better than a circulating-water mattress

NCT ID: NCT00710320 Completed - Hypothermia Clinical Trials

Temperature Changes During Induction of General Anesthesia in Pediatric Patients

Start date: July 2008
Phase: N/A
Study type: Observational

We aim that uncovering patients during induction of general anesthesia does not decrease core body temperature in pediatric patients.

NCT ID: NCT00676598 Completed - Cardiac Arrest Clinical Trials

A Prospective Analysis of the Effect of Therapeutic Hypothermia After Cardiac Arrest

Start date: January 2007
Phase: N/A
Study type: Observational

Therapeutic hypothermia has been shown to improve survival and neurologic outcome in patients resuscitated after ventricular fibrillation arrest. Few studies have examined whether therapeutic hypothermia is effective outside the research setting, or with other presenting rhythms. Our institution, a large community teaching hospital, instituted a therapeutic hypothermia protocol in November 2006 for all resuscitated cardiac arrest patients. The investigators seek to determine the mortality rate of our protocol and compare our complication rates with those of previously published studies.

NCT ID: NCT00676104 Completed - Clinical trials for Severe Traumatic Brain Injury

Discrete Hypothermia in the Management of Traumatic Brain Injury

Start date: July 2006
Phase: Phase 3
Study type: Interventional

The primary goal of this project is to demonstrate the feasibility and clinical benefits of a new rapid treatment for secondary treatment for secondary brain injury called Discrete Cerebral Hypothermia System by CoolSystems, Inc., Berkley, CA. This device induced hypothermia in the adult brain without significant whole body hypothermia. Discrete Cerebral Hypothermia System holds a great potential for protecting the brain from the devastating secondary complications of trauma without the associated deleterious system effects.