Professional Consequences of Ocular Trauma Hospitalized at the Hospital Centre of Clermont-Ferrand
NCT ID: NCT03706560
Last Updated: 2018-10-25
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
UNKNOWN
Total Enrollment
50 participants
Study Classification
OBSERVATIONAL
Study Start Date
2018-06-18
Study Completion Date
2023-02-28
Brief Summary
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Ocular trauma are a real public health issue. According to WHO, it is estimates at 750,000 hospital admissions per year in the world for ocular trauma, including 200,000 for open globe injuries in the world. Consequences can be severe with a significant number of definitive low vision or blindness which can lead to professionnal reclassifications for active patients. However, no study exists on professional consequences of those ocular trauma. Some studies showed that fonctionnal loss of an eye can also have psychological consequences such as post traumatic depression or can impair the quality of life but studies are scarce on this subject.
The primary objective is to study the professional reclassification of workers at least 6 months after their hospitalization for ocular trauma.
Secondary objectives are to assess, at least 6 months after an hospitalized ocular trauma, characteristics of eye injuries, characteristics of patients, mid-term consequences at work after eye injury and on personal aspects.
The primary objective is to study the professional reclassification of workers at least 6 months after their hospitalization for ocular trauma.
Secondary objectives are to assess, at least 6 months after an hospitalized ocular trauma, characteristics of eye injuries, characteristics of patients, mid-term consequences at work after eye injury and on personal aspects.
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Detailed Description
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Use of the ophthalmologic consultation report, the ophthalmologic hospitalization report and a telephone questionnaire to carry out the study.
At least 6 months after the traumatism, an ophthalmologist member of the team, M. Vincent Jawad, will call each patient for answering a telephone questionnaire after obtention of his oral consent.
If the traumatism occur after the beginning of the study, the patient will be informed, by M. Vincent Jawad, of the modalities of the study during his hospitalization and an information letter will be given to the patient in the same time (annex 2). His non opposition will be asked by telephone, remote from the hospitalization, before proceeding to the telephone questionnaire.
If the traumatism occur before the beginning of the study or if the information and non opposition letter has not been given to the patient during the hospitalization, the information letter (annex 2) will be sent by mail to the patient before the telephone call.
In all cases, the patient's consent (or non opposition) will be collected orally before proceeding to the telephone questionnaire (annex 1).
Medical data will be obtained from the medical report of hospitalization and the last report consultation of his ophthalmologist.
At least 6 months after the traumatism, an ophthalmologist member of the team, M. Vincent Jawad, will call each patient for answering a telephone questionnaire after obtention of his oral consent.
If the traumatism occur after the beginning of the study, the patient will be informed, by M. Vincent Jawad, of the modalities of the study during his hospitalization and an information letter will be given to the patient in the same time (annex 2). His non opposition will be asked by telephone, remote from the hospitalization, before proceeding to the telephone questionnaire.
If the traumatism occur before the beginning of the study or if the information and non opposition letter has not been given to the patient during the hospitalization, the information letter (annex 2) will be sent by mail to the patient before the telephone call.
In all cases, the patient's consent (or non opposition) will be collected orally before proceeding to the telephone questionnaire (annex 1).
Medical data will be obtained from the medical report of hospitalization and the last report consultation of his ophthalmologist.
Conditions
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Eye Injuries
Work Performance
Occupational Stress
Study Design
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Observational Model Type
COHORT
Study Time Perspective
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Adults, with a job
* hospitalized for ocular trauma in the ophthalmology unit of the University Hospital of Clermont-ferrand
* from january the first of 2005 to december the 31st of 2022.
* hospitalized for ocular trauma in the ophthalmology unit of the University Hospital of Clermont-ferrand
* from january the first of 2005 to december the 31st of 2022.
Exclusion Criteria
* Patient without job at the time of the ocular traumatism
* Refusal to participate in the study
* Unable to answer to the telephone questionnaire (difficulties understanding, cognitive disorders…)
* Impossibility to contact the patient
* Refusal to participate in the study
* Unable to answer to the telephone questionnaire (difficulties understanding, cognitive disorders…)
* Impossibility to contact the patient
Minimum Eligible Age
18 Years
Maximum Eligible Age
70 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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University Hospital, Clermont-Ferrand
OTHER
Sponsor Role
lead
Responsible Party
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Responsibility Role
SPONSOR
Principal Investigators
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Frédéric DUTHEIL, MD,PhD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Clermont-Ferrand
Locations
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CHU de Clermont-Ferrand
Clermont-Ferrand, Auvergne, France
Site Status
RECRUITING
Countries
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France
Central Contacts
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Facility Contacts
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References
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Other Identifiers
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2018-A00605-50
Identifier Type: OTHER
Identifier Source: secondary_id
CHU-399
Identifier Type: -
Identifier Source: org_study_id
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