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Evaluation of a Specialized Therapeutic Care of Patients Presenting an Intolerance Attributed to Electromagnetic Fields

NCT01854801 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 79

Last updated 2025-11-20

No results posted yet for this study

Summary

The purpose of the study is to evaluate efficacy of a 14 months follow-up and individual medical care of electro-sensitive patients: by measurement of health status, sensitivity to electromagnetic fields exposures, and quality of life.

Conditions

  • Idiopathic Environmental Intolerance Attributed to Electromagnetic Fields

Interventions

OTHER

Individual medical Care

Individual medical care in occupational and environmental diseases centers

OTHER

Individual electromagnetic exposures

During 7 days, patient hold a dosimeter measuring their electromagnetic exposures for FM, TV, GSM, DECT, WIFI, TETRA and relay antenna emissions. During this week, patients notify intensity and time of their symptoms on a self-questionary

Sponsors & Collaborators

  • ANSES, France

    collaborator UNKNOWN

  • INERIS, Verneuil-En-Halatte, France

    collaborator UNKNOWN

  • URC-CIC Paris Descartes Necker Cochin

    collaborator OTHER

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Lynda BENSEFA-COLAS, MD · Service de Pathologie Professionnelle, Hopital Cochin, AP-HP, Paris

  • Rene de SEZE, MD · INERIS (Institut National de l'EnviRonnement Industriel et des RisqueS)

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-09
Primary Completion
2015-05-30
Completion
2016-04-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01854801 on ClinicalTrials.gov