Trials / Completed
CompletedNCT06657352
Skin Efficacy Testing of Astrion Products
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 150 (actual)
- Sponsor
- Chia Nan University of Pharmacy & Science · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
This project aims to conduct safety and efficacy tests on the skin for the ingestion of Astrion Vitality Capsules, containing A. membranaceus and C. Asiatica roots, and the topical application of Astrion Vitality Cream. The goal is to develop health and skincare products that regulate physiological functions, promote overall wellness, and enhance skin beauty.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | ACS Topical Treatment Group | The topical group applied the ACS cream to the face twice daily (morning and night) for 4 weeks. |
| DIETARY_SUPPLEMENT | Topical Placebo Group | The topical group applied the cream (without ACS) to the face twice daily (morning and night) for 4 weeks. |
| DIETARY_SUPPLEMENT | Oral Treatment + Topical Treatment Group | The combination group used both the topical and oral ACS products for 12 weeks. |
| DIETARY_SUPPLEMENT | ACS Oral Treatment Group | The oral group ingested one ACS capsule twice daily after breakfast and dinner for 12 weeks. |
| DIETARY_SUPPLEMENT | Oral Placebo Group | The oral group ingested one capsule (without ACS) twice daily after breakfast and dinner for 12 weeks. |
| DIETARY_SUPPLEMENT | Oral Treatment + Topical Placebo Group | The combination group used both the topical and oral products without ACS for 12 weeks. |
Timeline
- Start date
- 2022-11-28
- Primary completion
- 2023-09-30
- Completion
- 2023-09-30
- First posted
- 2024-10-24
- Last updated
- 2024-10-26
Locations
1 site across 1 country: Taiwan
Source: ClinicalTrials.gov record NCT06657352. Inclusion in this directory is not an endorsement.