About this trial
The goal of this pilot, clinical, experimental, biological and prospective study with uso of biological material (venous blood sampling), in patient with acute carbon monoxide (CO) intoxication and in a group of healthy non-intoxicated subject (group of control) is the research of a possible increase of circulating microparticles level in human blood with an acute carbon monoxide intoxication.
The main question to answer is:
Is there an increase of circulating microparticles levels in subjects with acute carbon monoxide poisoning? Two blood samples will be withdrawn from patients with acute carbon monoxide poisoning, one before and one after hyperbaric oxygen treatment.
Researchers will compare a group of healthy volunteers to see if there is a different in circulating microparticles blood level compared to patients with intoxication.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age > 18 years
Acute carbon monoxide poisoning
Need for treatment with hyperbaric oxygen
Disqualifiers
Patient reject to consent
Trial population
Patients with CO poisoning that need hyperbaric oxygen treatment and afferent to the Hyperbaric center of the Nursing Home Habilita "I Cedri" located in Fara Novarese (NO). For every two intoxicated patients it will be necessary identify a healthy volunteer (matching 2:1) comparable with the patient intoxicated by sex, age (+/- 5 years), cigarette smoke.
Trial design
Case-control
Prospective
Treatments tested in this trial
Microparticles research
Diagnostic testThe absolute count of the total circulating microparticles will be carried out on the patients' plasma using the NanoSight NS300 instrument (Alphatest). Furthermore, the circulating microparticles will be stained with a combination of three monoclonal antibodies (Becton and Dickinson, NJ,USA) to detect microparticles released by the most abundant cell populations in the blood: leukocyte-derived microparticles (CD45+), endothelial-derived microparticles (CD31+), and PLT-derived microparticles (CD31+ CD41a+).
Treatment groups
Trial outcomes
Primary outcomes
Microparticles research
Quantify the number and the type of circulating microparticles in subjects after carbon monoxide poisoning.
Secondary outcomes
Relationship between poisoning severity and circulating microparticles levels
Evaluate the possible relationship between carbon monoxide poisoning severity measured as COHb levels and circulating microparticles levels before and after hyperbaric oxygen treatment.
Risk factors of delayed neurological syndrome development
Research of risk factors of delayed neurological syndrome development and follow up with test of Pfeiffer.
Proteomic and transcriptomic analysis
Researche the type of microparticles with proteomic and transcriptomic analysis
Sponsors and contacts
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Azienda Ospedaliero Universitaria Maggiore della Carita
Lead sponsor
Università degli Studi del Piemonte Orientale Amedeo Avogadro
Collaborator