Status:
UNKNOWN
Effects of Induced Moderate Hypothermia on ARDS Patients Under Venovenous ExtraCorporeal Membrane Oxygenation
Lead Sponsor:
Central Hospital, Nancy, France
Conditions:
ARDS, Human
Extracorporeal Membrane Oxygenation Complication
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Acute respiratory distress syndrome (ARDS) is a lesional pulmonary edema that occurs as a result of direct or indirect lung injury. This condition accounts for 10-15% of ICU admissions and 20-25% of p...
Detailed Description
The investigators propose a pilot study, monocentric, prospective, controlled, randomized, to apprehend in an objective and reliable way the effects of induced moderate hypothermia at 34°C, or at 33°C...
Eligibility Criteria
Inclusion
- Patients 18 years of age and older
- Intubated, ventilated patients with ARDS requiring VV ECMO
- Family member or trusted person who has been informed about the study and signed the informed consent form or inclusion in an immediate life-threatening situation
- Benefiting from a Social Security affiliation scheme
Exclusion
- Presence of a recirculation phenomenon (distance between the 2 ECMO cannulas \< 10 cm).
- Patients expected to die within 48 hours of VV ECMO implantation
- Patients on short-acting beta blockers
- Pregnant, parturient or lactating woman,
- Persons deprived of their liberty by a judicial or administrative decision,
- Minors (non emancipated)
- Adults subject to legal protection measures (guardianship, curatorship, safeguard of justice).
- Person undergoing psychiatric care under articles L3212-1 and L3213-1 of the french Public Health Code
Key Trial Info
Start Date :
September 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2024
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT05306392
Start Date
September 1 2022
End Date
September 1 2024
Last Update
April 1 2022
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