Evaluation of the Interest of a Specialist in Dermatology for Dermatopediatric Consultations (HLSkinPed)
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| ClinicalTrials.gov Identifier: NCT03578718 |
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Recruitment Status : Unknown
Verified June 2018 by Central Hospital, Nancy, France.
Recruitment status was: Not yet recruiting
First Posted : July 6, 2018
Last Update Posted : July 6, 2018
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Dermatologic diseases, of very different etiology and variable severity, represent a major motivation for consultation (in private consultations and in emergency departments), thus leading pediatricians to frequently turn to dermatologic advice.
The principal aim is to estimate the degree of concordance of the main diagnosis between a pediatrician and a pediatric dermatologist.
The secondary aims is to estimate the degree of concordance of the treatment, advices and follow-up.
| Condition or disease |
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| Dermatologic Disease Pediatric ALL Collaboration |
| Study Type : | Observational |
| Estimated Enrollment : | 100 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Official Title: | Evaluation of the Interest of a Specialist in Dermatology for Dermatopediatric Consultations |
| Estimated Study Start Date : | June 25, 2018 |
| Estimated Primary Completion Date : | May 1, 2019 |
| Estimated Study Completion Date : | May 1, 2019 |
- principal diagnosis [ Time Frame: baseline ]% of concordance between diagnosis (dermatologist/pediatric)
- treament [ Time Frame: baseline ]% of concordance between treatment (dermatologist/pediatric)
- advices [ Time Frame: baseline ]% of concordance between advices(dermatologist/pediatric)
- follow-up [ Time Frame: baseline ]% of concordance between follow-up (dermatologist/pediatric)
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| Ages Eligible for Study: | up to 18 Years (Child, Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Under 18 years old
- consultating for dermatologic problem in emergency department (1 department) or private pediatric center (1 center)
- signed consent
- consécutives consultations
Exclusion Criteria:
- no consent
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03578718
| Contact: BURSZTEJN Anne Calire, MCU-PH | +3383157153 | ac.bursztejn@chru-nancy.fr |
| Responsible Party: | Central Hospital, Nancy, France |
| ClinicalTrials.gov Identifier: | NCT03578718 |
| Other Study ID Numbers: |
2018-A00088-47 |
| First Posted: | July 6, 2018 Key Record Dates |
| Last Update Posted: | July 6, 2018 |
| Last Verified: | June 2018 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Skin Diseases |

