Evaluation of Human Efficacy of SOD Like Super Drink

TCI

Status: Completed

Conditions: Dermatology

Treatments: Dietary Supplement: SOD like Super Drink; Dietary Supplement: placebo drink

Study type: Interventional

Funder types: Industry

Identifiers

NCT06322589

CMUH112-REC3-175

Details and patient eligibility

About

To assess the efficacy of SOD like Super Drink on anti-oxidant capacity, immuno regulation and skin for human

Enrollment: 50 patients

Sex: All

Ages: 30 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• healthy adults aged between 30-65 years old

Exclusion criteria

• Subjects who have known cosmetic, drug or food allergies, difficulty in digestive tract absorption or disorder
• Patients with diseases of the skin, liver, kidney.
• 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 (> 3 hr/week) in the past 4 weeks.
• Students who are currently taking courses taught by the principal investigator of this trial.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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50 participants in 2 patient groups, including a placebo group

placebo drink

Placebo Comparator group

Treatment:

Dietary Supplement: placebo drink

SOD like Super Drink

Experimental group

Treatment:

Dietary Supplement: SOD like Super Drink