Investigation of the Efficacies of a Resveratrol Formula on Improvement of Skin Conditions and Inflammatory Related Factors

TCI

Status: Completed

Conditions: Skin Conditions; Proinflammatory Cytokines

Treatments: Dietary Supplement: Placebo drink; Dietary Supplement: Resveratrol drink

Study type: Interventional

Funder types: Industry

Identifiers

NCT04456829

20-0-54-B

Details and patient eligibility

About

To assess a resveratrol formula on improvement of skin conditions and inflammatory cytokines in blood

Enrollment: 60 patients

Sex: All

Ages: 20+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy volunteers aged above 20 years old

Exclusion criteria

• Subject who is not willing to participate in this study.
• Patients with diseases of the skin, heart, liver, kidney, endocrine and other organs and patients with mental illness (according to medical history).
• Subjects who have known cosmetic, drug or food allergies, difficulty in digestive tract absorption or disorder.
• Female who is pregnant or nursing or planning to become pregnant during the course of the study.
• Received facial laser therapy, chemical peeling or UV overexposure in the past 4 weeks.
• Subjects who have large spots (area >3 square centimeter) or abnormal acne.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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60 participants in 2 patient groups, including a placebo group

Resveratrol drink

Experimental group

Treatment:

Dietary Supplement: Resveratrol drink

Placebo drink

Placebo Comparator group

Treatment:

Dietary Supplement: Placebo drink