Last updated: February 7, 2024
Sponsor: Prof. Olivier Gaide, MD-PhD
Overall Status: Active - Recruiting
Phase
N/A
Condition
N/ATreatment
5GFR2 non ionizing EMW exposure
Clinical Study ID
NCT05933954
CHUV-DD-00884-SEAWAVE-2023
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Participants will be recruited in accordance with European and Swiss standards for thefollowing groups: Healtyh volunteers or Dermatoporosis defined as a chronic skinfragility syndrome orGorlin Goltz Syndrome defined as OMIM 10940014, or FamilialCylindromatosis or SB Syndrome defined as OMIM 132700/60504114, or XPV defined as OMIM 27875014 or Atopic dermatitis defined as a chronic inflammatory skin diseasecharacterised by eczematous skin lesions and intense pruritus
- Able to give informed consent as documented by signature,
- Adults, from 18 to 80 yo, according to groups
Exclusion
Exclusion Criteria:
- Recent intense exposure to sun (defined as causing a sunburn, within the last 7 days)
- Pregnant (excluded with a pregnancy test) or lactating women,
- Patients taking anti-coagulants
- Clinically significant concomitant diseases (cutaneous exam by the specialist),
- Active enrolment in another clinical trial,
- Participants incapable of judgment or participants under tutelage.
Study Design
Total Participants: 42
Treatment Group(s): 1
Primary Treatment: 5GFR2 non ionizing EMW exposure
Phase:
Study Start date:
January 09, 2024
Estimated Completion Date:
July 01, 2025
Connect with a study center
CHUV
Lausanne, Vaud 1011
SwitzerlandActive - Recruiting
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