Actively Recruiting

Age: 18Years - 99Years
All Genders
Healthy Volunteers
NCT05591300

Microparticles Blood Level in Acute Carbon Monoxide Poisoning

Led by Azienda Ospedaliero Universitaria Maggiore della Carita · Updated on 2024-11-14

108

Participants Needed

1

Research Sites

154 weeks

Total Duration

On this page

Sponsors

A

Azienda Ospedaliero Universitaria Maggiore della Carita

Lead Sponsor

U

Università degli Studi del Piemonte Orientale Amedeo Avogadro

Collaborating Sponsor

AI-Summary

What this Trial Is About

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 Two blood samples will be withdrawn from patients with acute carbon monoxide poisoning, one before and one after hyperbaric oxygen treatment.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

CONDITIONS

Official Title

Microparticles Blood Level in Acute Carbon Monoxide Poisoning

Who Can Participate

Age: 18Years - 99Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18 years
  • Acute carbon monoxide poisoning
  • Need for treatment with hyperbaric oxygen
Not Eligible

You will not qualify if you...

  • Patient reject to consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

AOU Maggiore della Carità

Novara, Italy, 28100

Actively Recruiting

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Research Team

R

Rosanna Vaschetto

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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