Microparticles Blood Level in Acute Carbon Monoxide Poisoning

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorAzienda Ospedaliero Universitaria Maggiore della Carita

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 Two blood samples will be withdrawn from patients with acute carbon monoxide poisoning, one before and one after hyperbaric oxygen treatment.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 volunteers

Qualifiers

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

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Microparticles research

    Diagnostic test

    The 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

108 Participants
are divided into 2 treatment groups
Group A: Patients1 intervention
Group B: Healthy controls1 intervention

Trial outcomes

Primary outcomes

1

Microparticles research

Quantify the number and the type of circulating microparticles in subjects after carbon monoxide poisoning.

Time frame
2 years

Secondary outcomes

1

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.

Time frame
45 days
2

Risk factors of delayed neurological syndrome development

Research of risk factors of delayed neurological syndrome development and follow up with test of Pfeiffer.

Time frame
45 days
3

Proteomic and transcriptomic analysis

Researche the type of microparticles with proteomic and transcriptomic analysis

Time frame
2 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Azienda Ospedaliero Universitaria Maggiore della Carita

Lead sponsor

Università degli Studi del Piemonte Orientale Amedeo Avogadro

Collaborator