Quantitative Sensory Testing in Subjects With Sensitive Skin or Not

NCT ID: NCT03081403

Last Updated: 2025-02-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-04-14

Study Completion Date

2017-10-27

Brief Summary

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Sensitive skin is a common problem, with 50% of women and 30% of men in Europe feel they have sensitive skin.

The Quantitative sensory testing (QST) is a physico-psychic method that uses gradients stimuli of different modalities to measure a subjective somatosensory response. This allows to characterize sensory dysfunction by assessing the participation of small and large nerve fibers.

The aim of this project is to characterize the presence or absence of a neurological disorder in patients with sensitive skin. This discovery would be a decisive argument to reinforce the suspicion that sensitive skins is linked to a small fiber neuropathy.

Detailed Description

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Sensitive skin is a common problem, with 50% of women and 30% of men in Europe feel they have sensitive skin. A sensitive skin is characterized by the occurrence of tingling sensations, tightness, heat, burning, itching or pain triggered by non pathogenic factors such as wind, heat, cold, water , cosmetics, toiletries, stress...

The Quantitative sensory testing (QST) is a physico-psychic method that uses gradients stimuli of different modalities to measure a subjective somatosensory response. This allows to characterize sensory dysfunction by assessing the participation of small and large nerve fibers.

The aim of this project is to characterize the presence or absence of a neurological disorder in patients with sensitive skin. This discovery would be a decisive argument to reinforce the suspicion that sensitive skins is linked to a small fiber neuropathy.

Conditions

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Sensitive Skin

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Subjects with sensitive skin

Subjects with a score greater than 50 on the sensitive scale

Group Type OTHER

Quantitative Sensory Testing

Intervention Type DEVICE

Study of detection thresholds of vibration, cold and pain related to the heat in the dominant hand of the subjects through the QST.

Subjects without sensitive skin

Subjects with result lower than 20 on the sensitive scale

Group Type OTHER

Quantitative Sensory Testing

Intervention Type DEVICE

Study of detection thresholds of vibration, cold and pain related to the heat in the dominant hand of the subjects through the QST.

Interventions

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Quantitative Sensory Testing

Study of detection thresholds of vibration, cold and pain related to the heat in the dominant hand of the subjects through the QST.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Age: between 20 and 60 years
* Cooperating patient
* Informed and written consent of the subject
* Affiliated to the social security
* For subjects with sensitive skin:

subjects with a score greater than 50 on the scale sensitive scale

\- To control subjects: subjects with result of less than 20 sensitive to the scale scale

Exclusion Criteria

* Adults subject with legal protection
* Subject in a social institution.
* Subject with major cognitive or psychiatric disorders
* Subject with pathological use of alcohol or consumption of another drug.
* Subject with skin involvement of the back of the dominant hand or malformation.
* Known sensitive neuropathy
* Pregnant woman
* Subject receiving medical treatment which may interfere with the results.
* Subject with treatment in the back of the dominant hand.
Minimum Eligible Age

20 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Brest

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHRU de Brest

Brest, , France

Site Status

Countries

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France

Other Identifiers

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SENSISKIN 29CRB16.0100

Identifier Type: -

Identifier Source: org_study_id

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