Study Results
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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COMPLETED
940 participants
OBSERVATIONAL
2021-06-15
2023-05-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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acute pain of pulpal origin
no intervention
questionnaire
questionnaires of precarity, dental anxiety, self medication, pain
anxious group
no intervention
questionnaire
questionnaires of precarity, dental anxiety, self medication, pain
Interventions
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questionnaire
questionnaires of precarity, dental anxiety, self medication, pain
Eligibility Criteria
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Inclusion Criteria
* Understanding and practicing French
* giving informed consent to participate in research.
* Affiliation to a Social Security scheme.
Exclusion Criteria
* Patient's refusal to participate in the study.
18 Years
ALL
No
Sponsors
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University Hospital, Clermont-Ferrand
OTHER
Responsible Party
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Principal Investigators
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Pierre-Yves Cousson
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Clermont-Ferrand
Locations
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CHU de Clermont-Ferrand
Clermont-Ferrand, , France
Countries
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Other Identifiers
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2021-A00417-34
Identifier Type: OTHER
Identifier Source: secondary_id
RNI 2021 COUSSON
Identifier Type: -
Identifier Source: org_study_id
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