Sensitive Skin

7

Review clinical trials related to Sensitive Skin. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Dermal Acceptability Evaluation in Sensitive Skin

The goal of this clinical trial is to evaluate the dermatological safety and acceptability of a cosmetic product in participants with sensitive skin. The main questions it aims to answer are: * Does the investigational product demonstrate dermatological acceptability in participants with sensitive skin under normal conditions of use? * Does the investigational product present a low risk of skin irritation? * What discomfort sensations, if any, are reported by participants with sensitive skin during product use? Participants will: * Apply the investigational product to the face and body twice daily under normal conditions of use. * Undergo clinical dermatological evaluations to assess signs of irritation and product tolerability. * Report any discomfort sensations experienced during the study period. The study will enroll 33 healthy male and female participants aged 18 years or older with sensitive skin confirmed by a positive Stinging Test. This is a single-center, single-blind clinical trial designed to evaluate the dermatological safety of the investigational product through clinical dermatological assessments under real-world conditions of use.

Participants needed: 33
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Brainfarma Industria Química e Farmacêutica S/AUpdated: Sep 30, 2026Locations: 1
Eligibility criteria

Male and female participants aged 18 years or older. [+5]

Pregnant or breastfeeding women, or women at risk of becoming pregnant during th... [+11]

Status: Recruiting

Dermal and Ophthalmological Acceptability Assessment in Sensitive Skin

This is a single-center, single-blind clinical study designed to evaluate the safety of the investigational product through dermatological and ophthalmological clinical assessments. A total of 33 female participants, aged 18 to 60 years, with a clinical diagnosis of sensitive skin confirmed by the Stinging Test, will be enrolled. Safety evaluations will be performed throughout the study period using standardized clinical assessments.

Participants needed: 33
Trial details
Age: 18-60Biological sex: FemaleType: InterventionalSponsor: Brainfarma Industria Química e Farmacêutica S/AUpdated: Sep 11, 2026Locations: 1
Eligibility criteria

Female participants aged 18 to 60 years. [+5]

Pregnant or breastfeeding women, or women at risk of becoming pregnant during th... [+16]

Status: Recruiting

A Clinical Investigation of a Topical Moisturizer on Skin Barrier Function in Adults With Sensitive Skin

The purpose of this research study is to evaluate whether a marketed moisturizing cream can improve skin barrier function (how well the outer layer of the skin keeps moisture in and protects the skin), skin hydration, skin sensitivity, inflammatory biomarkers (proteins in the skin that can provide information about inflammation), and the skin microbiome (the microorganisms that naturally live on the skin) in adults with sensitive skin, when compared with a commonly used moisturizing ointment (White Petrolatum) a widely used occlusive ointment (an ointment that forms a protective layer over the skin to help reduce moisture loss).

Participants needed: 24
Trial details
Phase: Phase 4Age: 18-55Biological sex: AllType: InterventionalSponsor: Good Molecules, LLCUpdated: Sep 10, 2026Locations: 1
Eligibility criteria

Adults aged 18 to 55 years, inclusive, of any sex. [+9]

Pregnancy, breastfeeding, or planning pregnancy during the study. [+18]

Status: Recruiting

Evaluation of Oral Collagen Peptides on Skin Barrier Function in Women

This clinical study aims to determine whether taking two different doses of collagen-derived peptides for three months improves facial skin barrier integrity in women with dry, sensitive skin, compared with a placebo.

Participants needed: 75
Trial details
Age: 45-70Biological sex: FemaleType: InterventionalSponsor: Centre de Pharmacologie Clinique Applique a la DermatologieUpdated: May 12, 2026Locations: 1
Eligibility criteria

Participant having signed an Informed Consent Form (ICF); [+8]

Participant with a BMI ≤17 or ≥30 kg/cm²; [+16]

Status: Not yet recruiting

Instant Flush Redness Clinical Efficacy Study

The goal of this clinical trial is to learn if an anti-redness emulsion can help lower facial redness caused by heat in healthy adult women. The main questions it aims to answer are: * Does the anti-redness emulsion lower facial redness better than purified water? * Is the product safe and comfortable to use? Researchers will compare the anti-redness emulsion to purified water using a split-face method. Participants will: * Receive infrared light on their face to trigger redness * Apply the anti-redness emulsion to one side of their face and purified water to the other side * Have their facial redness measured at different time points using photography, imaging devices, and skin redness tests * Answer questions about their experience with the products

Participants needed: 60
Trial details
Age: 20-40Biological sex: FemaleType: InterventionalSponsor: ChinaNormUpdated: Jul 16, 2025Locations: 1
Eligibility criteria

Chinese women aged from 20-40 years old. [+7]

Allergic to infrared light [+15]

Status: Not yet recruiting

A Clinical Study to Assess the Safety and Effectiveness of Test Product in Healthy Adult Human Subjects With Dry or Sensitive Skin

This exploratory, prospective, open-label, single-centre, safety, efficacy and in-use tolerability study of the test product in healthy adult human subjects with dry or sensitive skin.

Participants needed: 32
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: SAVA Healthcare LimitedUpdated: Apr 24, 2025Locations: 1
Eligibility criteria

Age: 18 to 55 years (both inclusive) at the time of consent. [+11]

History of any dermatological condition of the skin diseases. [+12]