Topical and Oral Regimen for Skin Health
Completed · Not applicable
Conditions studied: Skin Abnormalities
In brief
The overall objective of this study is to assess how oral supplementation with Inner Calm and the use of topical Super Calm can affect the appearance of skin and inner wellness, such as redness, skin sensitivity, and reactionary skin.
Key facts
- Study ID
- NCT04872946
- Run by
- Integrative Skin Science and Research
- People needed
- 74
- Starts
- 2019-11-26
- Expected to finish
- 2020-05-07
- Last updated by the study team
- 2021-05-05
Who can join
Age: 18 and older, up to 55. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Women aged 18-55
- Fitzpatrick skin type 1-4
- Self-perception as sensitive skin
You may not qualify if…
- Exclusion Criteria:
- Adults unable to consent
- Individuals who are not yet adults (infants, children, teenagers)
- Pregnant or breast-feeding women
- Prisoners
- Those who have used isotretinoin in the last 6 months
- Those who have used products containing salicylic acid, beta hydroxyl acids or vitamins A, C, or E or topical retinoids or topical depigmenting agents (such as hydroquinone, kojic acid, azelaic acid, or others in opinion of the investigator) in the last 14 days
- Those who are currently smoking or have smoked within the past 3 years.
- Those who have had a recent surgical or cosmetic procedure in the last 3 months that can affect facial wrinkles, redness, or hyperpigmentation, such as botulinum toxin injections, chemical peels, laser-based therapies to the face, or face lift surgeries
- Subjects with known allergy to any of the components of Inner Calm or Skin Calm
- Those that are unwilling to discontinue use of any other nutritional supplements including antioxidants, herbs, or protein-based supplements for 2 weeks prior to and during their participation.
- Subjects with a diagnosis of acne
Where it is running
- Integrative Skin Science and Research — Sacramento, California, United States
Full record on ClinicalTrials.gov
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