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Assessment of Nerve Damage Biomarkers in Acute and Chronic Organophosphate Toxicity

Recruiting
Conditions
Nerve Injury
Nerve Degeneration
Neuroinflammatory Response
Neurotoxicity
Nerve Damage
Genotoxicity
Interventions
Other: exposure to organophosphates
Registration Number
NCT06021262
Lead Sponsor
Alexandria University
Brief Summary

The aim of this observational study is to answer the following questions in individuals with acute and chronic exposure to organophosphates. The main questions to be addressed are

1. What are the prognostic values of neuroinflammatory markers?

2. What are the genotoxic effects of organophosphates?

3. what are the changes occurring in the levels of traditional oxidative stress and inflammatory markers?

Detailed Description

This is a cross-sectional study that aims to assess the possible prognostic value of markers of neuroinflammation and nerve damage in patients with acute and chronic exposure to organophosphate pesticides by conducting a full proteomic and metabolomic profile. The possible genotoxic effect of common organophosphate pesticides will be studied as well. This will be conducted in parallel to the assessment of traditional markers of inflammation and oxidative stress. The target populations are patients with acute and chronic exposure to organophosphates with a total estimated number of 90 including individuals assigned to the control group with matched age and gender.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
90
Inclusion Criteria
  • For the control group: healthy individuals without previous exposure to organophosphates, with the specified age limits.
  • For the acute exposure group: patients with acute exposure to organophosphates, with the specified age limits
  • For the chronic exposure group: patients with chronic exposure to organophosphates, with the specified age limits

No restrictions on comorbidities in the three groups except those mentioned under Exclusion Criteria

Exclusion Criteria
  • Pediatric patients.
  • Patients with neurological diseases (Parkinsonism, epilepsy, Alzheimer's disease, etc.)
  • Patients who does not meet the inclusion criteria.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
chronic exposure groupexposure to organophosphatespatients with chronic occupational or environmental exposure to organophosphates
acute exposure groupexposure to organophosphatespatients with acute exposure to organophosphates in accidental or suicidal settings
Primary Outcome Measures
NameTimeMethod
Identification of neuroinflammatory biomarker1.5 years

The biomarker should correlate with nerve injury

Identification of the mechanism of neuroinflammation1.5 years

To detect the possible pathways involved in initiation of systemic inflammation rather than inhibition of choline esterase enzyme. As well as, studying the possible relation of these identified mechanisms with neuronal inflammation and damage.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Alexandria Main University Hospital

🇪🇬

Alexandria, Egypt

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