Hopital Cochin - Service de Medecine intensive et reanimation au 27 rue du Faubourg Saint-Jacques
Paris, 75014, France
Location contact
Alain Cariou, M.D.
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06798818
Out-of-hospital cardiac arrest (OHCA) affects over 356,000 individuals annually in the United States, with fewer than 10% surviving to hospital discharge, mirroring statistics from Europe. Post-cardiac arrest syndrome (PCAS), a condition causing multi-organ dysfunction, is a leading cause of mortality despite successful resuscitation efforts. Targeted temperature management (TTM) is recommended for comatose patients post-resuscitation to mitigate PCAS, but optimal temperature targets and cooling methods remain unclear. Experimental studies suggest that therapeutic hypothermia (32-34°C), induced rapidly after resuscitation, may provide significant clinical benefits.
Total liquid ventilation (TLV) with breathable liquids has been proposed to achieve ultra-rapid therapeutic hypothermia (URTH). This approach uses the lungs as a heat exchanger to achieve ultra-rapid cooling while maintaining normal gas exchange. It enables a reduction in core body temperature to the hypothermic range (33.0 ± 0.5°C) within 45 minutes in relevant experimental models.
The OverCool study is an open-label, single-arm, multi-centric pilot trial designed to evaluate the performance and safety of Vent2Cool, a medical device intended to induce ultra-rapid therapeutic hypothermia by TLV in resuscitated cardiac arrest patients. The primary objective is to demonstrate Vent2Cool's ability to achieve a target core temperature of 33.0 ± 0.5°C within 60 minutes from start of procedure in resuscitated patients admitted to the Intensive Care Unit following intra- or extra-hospital cardiac arrest. Secondary objectives include assessing procedural safety, cooling performance, feasibility in emergency settings, clinical outcomes, and the impact on biological markers.
Trial opening soon.
Get Notified18 year–84 year
All sexes
Interventional
Not applicable
Paris, 75014, France
Alain Cariou, M.D.
PRINCIPAL_INVESTIGATOR
The "American Heart Association's 2022 Update" estimates that over 356,000 out-of-hospital cardiac arrests (OHCA) occur annually in the United States. These figures are consistant with data from European countries, where fewer than 10% of OHCA patients survive, despite 30% being successfully resuscitated before admission to intensive care units (ICU). The majority of these patients succumb to post-cardiac arrest syndrome (PCAS), a condition characterized by multi-organ failure.
To mitigate the severity of PCAS, current guidelines recommend continuous core temperature monitoring and active fever prevention through targeted temperature management (TTM) in patients who remain comatose following resuscitation from cardiac arrest. While TTM with a target temperature range of 32-36°C has been previously evaluated and applied in specific subpopulations, there is insufficient evidence to universally recommend one target temperature over another within this range. Conversely, experimental studies have demonstrated that the protective effects of therapeutic hypothermia (32-34°C) are strongly influenced by the rate of cooling initiated after resuscitation. These findings suggest that very early application of hypothermia may provide greater benefits compared to simply avoiding fever, emphasizing the importance of timely intervention.
In this context, Total Liquid Ventilation (TLV) with breathable liquids has been investigated in animal studies as a method to achieve ultra-rapid therapeutic hypothermia (URTH) following cardiac arrest. This innovative approach uses the lungs as a potent heat exchanger to achieve ultra-rapid cooling while preserving normal gas exchanges. TLV has demonstrated the capability to lower body core temperature from normothermia to the hypothermic range within 45 minutes, irrespective of body weight, in relevant experimental models. Furthermore, unlike earlier techniques of partial liquid ventilation, this method employs a lung-conservative liquid ventilation approach, which has been shown to be safe. The objective of the present OverCool study is to evaluate the performance and safety of the Vent2Cool device, designed to induce URTH by TLV safely following cardiac arrest.
Accordingly, OverCool is an open-label, single arm, non-comparative, multi-centric pilot study. The study primary objective is to demonstrate the ability of Vent2Cool to achieve a core body temperature of 33.0±0.5°C in less than 60 min after the start of the procedure in resuscitated patients admitted in the ICU after an intra- or extra-hospital cardiac arrest. The main secondary objectives are to demonstrate the safety of the procedure, the cooling performance, the ability to implement the procedure in the emergency setting of post-cardiac arrest management, the clinical outcomes and impact on biological markers.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Vent2Cool System is a targeted temperature management device used to induce ultra-rapid therapeutic hypothermia by total liquid ventilation.
Time frame: From start of Vent2Cool procedure to 60min after
The primary end point is the success of the procedure. The success of the procedure is defined as the ability to reach a body core temperature (bladder temperature recommended) of 33.0±0.5°C and a safe return to conventional mechanical ventilation within less than one hour after Vent2Cool start. Start of the Vent2Cool procedure is defined as the opening of the Vent2Cool patient connector valve.
Time frame: At Day 28
mRS will be evaluated at Day 28. The modified Rankin Scale is a scoring system on neurologic function ranging from 0-6, where 0 means no symptoms at all, higher numbers indicating increasing neurologic disabilities and 6 equals death.
Time frame: From start of Vent2Cool procedure to 37 hours after
Core temperature (bladder recommended) at start of Vent2Cool procedure and for 36 h after the end of Vent2Cool procedure to include the maintenance and rewarming phases of TTM
Time frame: During the Vent2Cool procedure
Duration in minutes from start of the Vent2Cool procedure (i.e. opening of the Vent2Cool patient connector valve) to Body Core Temperature inferior or equal to 33,5 °C
Time frame: From ROSC to end of Vent2Cool procedure
Duration in minutes from ROSC to body core temperature inferior or equal to 33,5 °C
Time frame: Inclusion, 10 min and 25 min after start of Vent2Cool procedure
PaO2 and PaCO2 values from arterial blood gases sampled at inclusion and 10 and 25 minutes into the Vent2Cool procedure
Time frame: Until Day 28
Patient Vital status collected at ICU discharge and/or Hospital discharge (if before Day 28) and systematically at Day 28. In case of death : cause of death
Time frame: At Day 28
The Glasgow Outcome Scale (GOS) is an ordinal scale used to assess functional outcomes of patients following brain injury.
GOS includes five grades: 5, good recovery; 4, moderate disability; 3, severe disability; 2, persistent vegetative; and 1, death.
Time frame: During the Vent2Cool procedure
Cooling rate is expressed in °C/h and calculated as follows: temperature at start of Vent2Cool procedure - 33.5°C / duration to achieve a core temperature of 33.5°C
Time frame: From start of Vent2Cool procedure to 60min after.
Number and percentage of patients for whom the core temperature value is lower than 32°C and / or 30°C within 60 minutes after the start of the Vent2Cool procedure
Time frame: During the Vent2Cool procedure
Time frame: At inclusion
Value of the modified Cardiac Arrest Hospital Prognosis (mCAHP) Score. Scores of either <80; [80; 105[ or >105 predict of risk of poor outcomes of respectively at least 40%, at least 80% or at least 95%.
Time frame: At inclusion
Number of patients for which the mCAHP score predicted a poor outcome with a risk of at least 40 % (mCAHP <80), at least 80% (mCAHP [80; 105[) or at least 95 % (mCAHP ≥ 105) vs. the total number of patients within each mRS category at Day 28.
Time frame: At inclusion, Day1 and Day3
Time frame: At inclusion, Day 1 and Day 3
Time frame: At inclusion, 10 min and 25 min after start of Vent2Cool procedure
Time frame: At inclusion, 10 min and 25 min after start of Vent2Cool procedure
Time frame: During the Vent2Cool procedure
Time frame: During the Vent2Cool procedure
Time frame: Day 28
The images of the CT scans will also be kept for possible later centralized analyses, if necessary.
Time frame: At inclusion, at Day 3 and at Day 28.
Time frame: At Day 1 and Day 3
Time frame: At Day 3
Time frame: During Vent2Cool procedure.
Occurence of desaturation episodes defined as SpO2<75% on pulsed oxymeter lasting at least 5 minutes during Vent2Cool procedure.
Time frame: At inclusion, 10 min and 25 min after start of Vent2Cool procedure
Severe hypercapnia defined as PaCO2>75 mmHg, in blood gases sampled at 10 and 25 minutes after start of Vent2Cool
Time frame: At inclusion, 10 min and 25 min after start of Vent2Cool procedure
Severe hyperoxemia defined as PaO2>400 mmHg, in blood gases sampled at 10 and 25 minutes after start of Vent2Cool
Time frame: At inclusion, 10 min and 25 min after start of Vent2Cool procedure
Hypoxemia defined as PaO2 < 75 mmHg, in blood gases sampled at 10 and 25 minutes after start of Vent2Cool
Time frame: Day 1 to Day 3
Presence of pupillary light reflex and Neurological pupil index (NPi) at Day 1, 2 and 3
Time frame: From return of spontaneous circulation to start of Vent2Cool procedure
Duration in minutes from ROSC to start of the Vent2Cool TLV procedure
Time frame: From patient admission to ICU to start of Vent2Cool procedure
Time frame: From the start of the Vent2Cool procedure to the end of the procedure
Time during which the patient is ventilated by Vent2Cool form start of Vent2Cool to end of TLV by lung draining procedure.
Time frame: During Vent2Cool procedure.
based on device data recorded during the Vent2Cool procedure
Time frame: At 1h, 2h, 12h, 24h, 48h and 72h after the start of the Vent2Cool procedure
Including measured values of:
Time frame: Until Day 28
For patients discharged alive from hospital and / or alive at Day 28.
Contact information is provided by the study sponsor or research team.
Fabrice Paublant
CONTACT
Sandrine Perrotto, PhD
CONTACT
ORIXHA
Industry
Acronym: OverCool
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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