Actively Recruiting
Pathophysiological Study of the Sensitive Scalp
Led by University Hospital, Brest · Updated on 2026-05-08
40
Participants Needed
1
Research Sites
48 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Sensitive skin is defined as a syndrome manifested by the occurrence of unpleasant sensations (tingling, burning, pain, pins and needles) in response to stimuli that should not normally cause them. These unpleasant sensations cannot be explained by lesions attributable to a specific skin disease. Sensitive skin can affect different parts of the body. The scalp is a site that is often affected, with specificity linked in particular to the presence of hair and different triggering factors (styling habits, wearing of head coverings, application of cosmetics to the scalp, etc.). Sensitive scalp affects around half the population, and can have an impact on the quality of life of sufferers, particularly those whose symptoms are very intense. Women are more likely than men to have a sensitive scalp, so in order to have a more homogenous study population, we chose to include 40 women. The pathophysiology of sensitive skin is imperfectly understood, and studies specific to the sensitive scalp are very rare. However, the pathophysiology of the sensitive scalp could be different because it is a hairy area, more innervated, and less exposed to environmental factors.
CONDITIONS
Official Title
Pathophysiological Study of the Sensitive Scalp
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult women without dermatosis
- Provide free and informed consent
- Affiliated to a social security scheme
- Control group: Sensiscalp score = 0/20
- Sensitive scalp group: Sensiscalp score 23 3/20 with pruritus sensation 23 2/20
You will not qualify if you...
- Refusal to take part in the study
- Dermatosis of the scalp such as psoriasis or seborrhoeic dermatitis
- Pregnant or breastfeeding women
- Women under legal protection (guardianship, curatorship)
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Chu Brest
Brest, France, 29200
Actively Recruiting
Research Team
E
Emilie BRENAUT, Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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