- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03101761
Characteristics and the Future of the City Chilblains
Chilblains are cutaneous lesions affecting extremities (foot and fingers) with erythemic papules, evolving by painful relapse due to cold and sudden reheating.
This pathology is currently poorly understood while it's frequent.
The aim of the study is to evaluate all the characteristics of this pathology by reporting clinical and biological data of patient consulting for chilblains; and the other point is to assess the evolution of these patients.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Ile-de-France
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Paris, Ile-de-France, France, 75014
- Groupe Hospitalier Paris Saint Joseph
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- patient consulting for chilblains
- diagnostic of chilblain during the consultation
Exclusion Criteria:
- patients consulting for other reason than chilblains
- patient who can't reply by telephonic call
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Évaluation of chilblains' topography
Time Frame: Day 1
|
This assessment consists to evaluate the chilblains topography, vasospastic profile and presence or not of another acrosyndrome
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Day 1
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Questionnaire of assessment of chilblains' evolution
Time Frame: 2 months
|
2 months
|
Collaborators and Investigators
Investigators
- Study Director: Pascal PRIOLLET, MD, Groupe Hospitalier Paries St JOSEPH
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ENGELURES
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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