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Clinical Trials/NCT00864955
NCT00864955
Completed
Not Applicable

Damage to DNA Caused by UV-A Irradiation: Photochemical Mechanism and Cutaneous Parameters Involved in the Formation of Cyclobutane Pyrimidine Dimers

University Hospital, Grenoble2 sites in 1 country24 target enrollmentMarch 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy Volunteers
Sponsor
University Hospital, Grenoble
Enrollment
24
Locations
2
Primary Endpoint
Phototype determination according to the Fitzpatrick classification Number of CPD and oxidative lesions determinated by the analysis of DNA from the skin biopsies after their ex-vivo exposure to UV-A - The CPD / Oxidative lesions ratio
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The DIMUVA study aims to evaluate the correlation between cutaneous phototype and the nature and quantity of damage caused to cutaneous DNA after exposure to UV-A radiation.

Detailed Description

Due to their capacity to damage Deoxyribonucleic acid (DNA), Ultra-Violet (UV) radiation is one of the causes of skin cancers. Until recently, the genotoxic effects of UV-A radiation, were poorly identified, in particular their capacity to lead to the dimerization of pyrimidine bases . It is well known that the response to UV-A and UV-B radiations is different depending on the cutaneous phototype. Thus, the aim of this study is to determine the correlation between cutaneous phototype and the quantity and nature (CPD or oxidative lesions) of damage caused to cutaneous DNA after an ex-vivo exposure to UV-A and UV-B radiations.

Registry
clinicaltrials.gov
Start Date
March 2009
End Date
July 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
University Hospital, Grenoble

Eligibility Criteria

Inclusion Criteria

  • Between 18 and 35 years old,
  • Healthy volunteers,
  • Cutaneous phototype 2 or 4 according to the Fitzpatrick classification,
  • Affiliation to the French Social Security.

Exclusion Criteria

  • History of photosensibility,
  • Active smoking or stopped since less than one year,
  • Dermatological pathology or treatment contra-indicating cutaneous irradiation and skin biopsies,
  • Any chronic pathology susceptible to interfere with the evaluations related to the protocol,
  • Allergy to local anaesthetics,
  • Volunteers who take drugs and/or food complements acting on oxidative stress in the 8 weeks preceding inclusion,
  • Volunteers who have take paracetamol or aspirin within 7 days prior to the inclusion visit,
  • Subject in exclusion period for another biomedical research study,
  • Subject having exceeded the threshold of annual compensation for biomedical research.

Outcomes

Primary Outcomes

Phototype determination according to the Fitzpatrick classification Number of CPD and oxidative lesions determinated by the analysis of DNA from the skin biopsies after their ex-vivo exposure to UV-A - The CPD / Oxidative lesions ratio

Time Frame: Day 0

Secondary Outcomes

  • Number of CPD and oxidative lesions determinated by the analysis of DNA from the skin biopsies after their exposure ex-vivo to UV-B.(Day 0)
  • UV-A radiation exposure: Minimal erythemic dose - Number of CPD and oxidative lesions - CPD / oxidative lesions ratio(Day x)
  • UV-B radiation exposure: Minimal erythemic dose - Number of CPD and oxidative lesions - CPD/oxidative lesions ratio(Day 0)
  • antioxidant status and quantity of CPD, oxidative lesions after exposure to UV-A and UV-B radiations(day 2)

Study Sites (2)

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