Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05231681
Other study ID # 20231Saie
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 15, 2022
Est. completion date May 1, 2022

Study information

Verified date May 2022
Source Saie Beauty
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Saie Beauty has developed 'Hydrabeam Sheer Brightening Under Eye Concealer' that is specifically designed for improving under-eye skin health. The concealer is aimed at improving under-eye skin features including hydration, firmness/elasticity, smoothness, and brightness. At the same time, it is aimed at reducing imperfections such as dark circles, skin redness, fine lines, wrinkles, and crow's feet. The aim is to understand and assess the efficacy of treatment from the participants' perspective and to see if the participants reported changes in skin features, dark circles, brightness, fine lines, wrinkles, crow's feet, and other skin imperfections.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date May 1, 2022
Est. primary completion date May 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Female between 18 and 45 years old - Must be in good general health - Want to improve under-eye skin health by improving skin hydration, firmness/elasticity, smoothness, and brightness - May have dark circles, fine lines, wrinkles, and crow's feet - Must be willing to comply with the study protocol - Must be willing to add the concealer to their daily routine for the duration of the study - Must maintain a basic skincare routine, e.g., must use moisturizer and sunscreen daily - Able to communicate in English - Must provide a written Informed Consent Form (ICF) - Willing to share feedback via the given online portal Exclusion Criteria: - Unwilling to follow the routine of the study - Unwilling to provide informed consent - Currently participating in another research study - Severe chronic conditions including ontological and psychiatric conditions - Use of prescription medication relevant for the skin - Have any known allergies to the ingredients of the test product - Known to have any severe allergic reactions in the past - Undergoing any cosmetic procedures such as laser treatments, Botox, or chemical peels for the duration of the study. - Have diagnosed or self-identified sensitive skin - Have any learning and/or cognitive difficulties that prevent them from reading and understanding questionnaires and surveys (e.g. dementia) - Currently pregnant or breastfeeding, or want to become pregnant for the duration of the study - Use of prescription drugs (topical or oral) that are targeted at any sort of skin condition (for example retinoids)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Saie Beauty's Hydrabeam Sheer Brightening Under Eye Concealer
Eye Concealer

Locations

Country Name City State
United States Citruslabs Santa Monica California

Sponsors (1)

Lead Sponsor Collaborator
Saie Beauty

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Skin aging [Time frame: Baseline to 4 weeks] Patient reported outcome measures (Scale 0-5 with higher scores representing a better outcome) to assess the reduction of early signs of aging such as fine lines, dark spots, and brighter skin 4 weeks
See also
  Status Clinical Trial Phase
Completed NCT05098912 - Comparing Polydioxanone Thread Embedding Acupuncture and Manual Acupuncture for Nasolabial Fold Reduction N/A
Completed NCT05271136 - A Clinical Study to Evaluate the Efficacy of an Anti-Aging Serum N/A
Completed NCT05096247 - Post Market Study To Collect Efficacy Data For The Treatment Of Wrinkles With A Radiofrequency Device N/A
Completed NCT05097157 - Study To Assess A Radiofrequency Microneedling Device For Dermatologic Conditions N/A
Completed NCT04128046 - The Effect of Platelet-rich Fibrin Matrix on Skin Rejuvenation N/A
Active, not recruiting NCT04727099 - Clinical Evaluation to Demonstrate the Safety and Performance of the Candela PicoWay System™ N/A
Active, not recruiting NCT06140628 - A 28-day Clinical Study on Facial Skin Rejuvenation N/A
Not yet recruiting NCT05524779 - BTL-785F Device for Non-invasive Reduction of Wrinkles and Overall Facial Improvement N/A
Completed NCT05514782 - A Clinical Study to Evaluate the Long-Term Efficacy and Tolerability of a Daily Anti-Aging Daily Serum N/A
Completed NCT06123572 - A Clinical Study to Assess the Safety and Effectiveness of Anti-Ageing and Skin Brightening Gel N/A
Completed NCT04911374 - An Open-Label Clinical Study to Evaluate the Efficacy of a Face Cream and Eye Cream N/A
Recruiting NCT04989361 - Soluble Hyaluronic Acid Microneedle VS. Non-ablative Fractional Laser on Infraorbital Wrinkles. N/A
Recruiting NCT04540900 - A Phase I Study of KB301, a Replication-Incompetent, Non-Integrating Vector Expressing Human Type III Collagen (COL3) for the Treatment of Superficial Skin Depressions Phase 1
Recruiting NCT06202274 - Clinical Study to Evaluate the Safety and Efficacy of Candela Technology N/A
Recruiting NCT06074276 - The Effects of Almond on Facial Skin Collagen and Wrinkles N/A
Completed NCT06366503 - Evaluating Procedure Pairing of a Post-Procedure Cream Versus a Comparator in Patients Treated With Fractional Ablative CO2 Laser for Facial Rejuvenation N/A
Active, not recruiting NCT06219278 - A Retrospective Review Evaluating the Matrix Pro Applicator for Treatment of Wrinkles N/A
Active, not recruiting NCT06192550 - Functional Usability and Feasibility Testing of the Profound Matrix™ System N/A
Completed NCT04650620 - Study to Evaluate the Performance and Safety of the Medical Device Plenhyage® N/A
Completed NCT03729700 - The Effect of Almonds on Facial Aesthetics and Modulation of the Microbiome and Lipidome N/A