Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05328388
Other study ID # IRSI-E-ES-094155-01-10-21
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date March 15, 2022

Study information

Verified date July 2022
Source LycoRed Ltd.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will be performed with oral gels, with up to 55 study subjects who meet the inclusion and non-inclusion criteria required. Study subjects will be instructed to use the products during 12 weeks and they will be assessed and supervised throughout the study by clinic technicians, in order to check for possible adverse events. Efficacy documentation through digital photography, instrumental measurements with the devices Cutometer® MPA 580 and Tewameter®, image acquisition with Visia-CA® as well as self-assessment through questionnaires will be carried out.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 15, 2022
Est. primary completion date March 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 35 Years to 55 Years
Eligibility Inclusion Criteria: 1. Females in good general health, and between ages of 35 and 55 years old, inclusive at enrollment; 2. 50 subjects: 20 Caucasians + 10 Asians + 10 African Americans + 10 Latinos; 3. All Fitzpatrick skin types being II, III and IV for Caucasian/Asian; 4. Subjects to have Glogau skin classification of photoaging, Type 2; 5. Subjects with baseline signs of facial skin aging as conformed by visual expert grading of photographs Exclusion Criteria: 1. Subjects participating in any other clinical studies; 2. Subjects that underwent beauty injections/ deep pealing/ cosmetic surgery/ tanning- for 3 months before study starts and for all the study duration. 3. Subjects having an acute or chronic disease or medical condition, including dermatological problems, which could put her at risk in the opinion of the Principal Investigator or compromise study outcomes. Typical uncontrolled chronic or serious diseases and conditions which would prevent participation in any clinical trial are cancer, AIDS, diabetes (insulin dependent), renal impairment, mental illness, drug/alcohol addiction; 4. Unreliable or unlikely to be available for the duration of the study; 5. History of allergic reactions, skin sensitization and/or known allergies to cosmetic ingredients, toiletries, sunscreens, etc.; 6. Immunocompromised subjects

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Lycomato
Lycomato sof gels

Locations

Country Name City State
United States Media Lab Science Los Angeles California

Sponsors (1)

Lead Sponsor Collaborator
LycoRed Ltd.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Expert clinical grading of efficacy attributes Visual assessments will be performed by the expert grader using a 10-point ordinal scale on the face. 12 weeks
See also
  Status Clinical Trial Phase
Active, not recruiting NCT06140628 - A 28-day Clinical Study on Facial Skin Rejuvenation N/A
Not yet recruiting NCT06000163 - Normal Reference Values in Han Adults of Skin Thickness and Blood Flow by High-frequency Ultrasound
Completed NCT05844683 - Effect Of Bath Wıth Chlorexıdıne On Protectıon Of Skın Integrıty And Preventıon Of Hospıtal Infectıon N/A
Completed NCT04510103 - A Controlled Clinical Study of 2 Different Moisturizers for the Relief of Dry Skin N/A
Recruiting NCT04305691 - Trial of Ixazomib for Kaposi Sarcoma Phase 2
Not yet recruiting NCT03347448 - Multidimensional Cross-sectional Study on Skin Health Based on TCM Constitution - Psychology - Skin Model N/A
Completed NCT05011461 - The Effect of Topical Almond Oil vs. Topical Retinol on The Appearance of Facial Wrinkles N/A
Recruiting NCT06462690 - EFFECT OF CARE PROVIDED THROUGH SKIN CARE PROTOCOL ON ELDERLY PATIENTS N/A
Recruiting NCT03189628 - The Effect of Autologous Stromal Vascular Fractions on Skin Regeneration Phase 1/Phase 2
Recruiting NCT06066463 - My Skin & Hair Journey_virtual Registry
Recruiting NCT05033795 - Metabolomic Evaluation of the Impact of Acqua Rocchetta on the Skin of Healthy Patients. N/A
Completed NCT00698100 - Vaccination of AJCC Stage IIB, IIC, III and IV Melanoma Patients With Human and Mouse Tyrosinase DNA Vaccines Phase 1
Completed NCT05564624 - Effect of Fasting-Mimicking Diet on Skin Health N/A
Completed NCT05537350 - A Clinical Study to Evaluate the Efficacy and Consumer Perception of Lumenato N/A
Recruiting NCT05235997 - Placebo Controlled Efficacy Evaluation of the Hydrolyzed Collagen Peptide In Adult Females N/A
Completed NCT03887208 - Therapy of Scars and Cutis Laxa With Autologous Adipose Derived Mesenchymal Stem Cells Phase 1/Phase 2
Withdrawn NCT04356456 - A Double-Blind, Randomized, Placebo-Controlled Study Evaluating the Nutritional Supplement Lumenato and Its Impact on Skin Parameters in Healthy Female Subjects N/A
Completed NCT04248699 - Lumenato Nutritional Supplement on Skin Appearance N/A