Evaluation of the Effectiveness of the Anti-aging Effect of a Supplement in Improving Skin Conditions

Aging Well Clinical Trial

Official title:

Avaliação de eficácia do Efeito Antienvelhecimento de um Suplemento Alimentar na Melhora Das condições da Pele - Estudo Clínico, Subjetivo e Instrumental

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05879289
• Other study ID #: EN20-1103
• Status: Completed
• Phase: N/A
• Start date: January 25, 2022
• Est. completion date: May 17, 2022

Study information

• Verified date: May 2023
• Source: Farmoquimica S.A.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A unicentric, blind, non-comparative clinical study to evaluate facial and body anti-aging efficacy of a supplement in female participants through clinical, subjective and instrumental evaluations.

Description:

A unicentric, blind, non-comparative clinical study to evaluate facial and body anti-aging efficacy of a supplemente in female participants through clinical, subjective and instrumental evaluations.

It will be necessary 33 female participants aged between 35 and 60 years old with signs of aging on the face and neck, complaining of body flaccidity and gynoid lipodystrophy.

The participant will remain in the study for 90 days using the product. Visits will be scheduled in D0, D45 and D90.

Instrumental evaluations: Evaluated on each visit:

• Skin elasticity and firmness using Cutometer - D0, D45 and D90;

• Skin hydration using Corneometer- D0,D45 and D90;

• Detection and accuracy of fine lines and wrinkles using Visia -D0,D45 and D90

• Dermal thickness and density in the thigh region using Ultrasound Voluson E8 before using the product (D0) and after 90 (D90) days of continuous use;

• Participants will respond to a subjective assessment using a questionnaire to capture possible feelings of discomfort during the study and subjective efficacy.

• A dermatologist will be available to monitor the participants throughout the study and respond an assessment of clinical efficiency

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: May 17, 2022
• Est. primary completion date: May 17, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 35 Years to 65 Years

Eligibility

Inclusion Criteria:

• Signs of aging in the face and neck region (fine lines, furrows and expression lines);

• Participants with complaints of body sagging;

• Participants with BMI < 30 (body mass index less than 30);

• Participants with Gynoid Lipodystrophy Grade 1 and/or 2;

• Agreement to follow the trial procedures and attend the clinic on the days and times determined.

• Ability to understand and consent to their participation in this clinical study, manifested by signing the Term of Free and Informed Consent (TCLE)

Exclusion Criteria:

• Participants who have been diagnosed with COVID-19 by RT-PCR examination or by the presence of IgM antibodies in the serology exam, in the last 4 weeks or who are presenting any of the following symptoms: dry or productive cough, sneezing, runny nose, body ache, headache, anosmia (loss of smell), ageusia (loss of taste) and/or any other symptoms that may be related to covid-19 at the discretion of the investigator;

• Pregnancy or risk of pregnancy/lactation;

• Use of the following topical or systemic medications: immunosuppressants, antihistamines, anti-inflammatories non-hormonal drugs, and corticoids up to 30 days before selection or considering immunosuppressants, the interval should be 3 months before selection;

• Atopic or allergic history to Food Supplements;

• Pathologies and/or active skin lesions (local and/or disseminated) in the assessment area;

• Skin marks in the experimental area that interfere with the evaluation of possible skin reactions (malformations vascular lesions, scars, increased hairiness, large nevus, sunburn);

• Immunosuppression by drugs or active diseases;

• Decompensated endocrinopathies;

• Participants with known congenital or acquired immunodeficiency;

• Relevant medical history or current evidence of alcohol or other drug abuse;

• Known history or suspected intolerance to products of the same category;

• Intense sun exposure up to 15 days before the evaluation;

• Aesthetic or dermatological treatment in the evaluation areas up to 04 weeks before selection;

• Professionals directly involved in carrying out this study;

• Other conditions considered by the evaluating physician as reasonable for disqualification from participation in the study. If so, it should be described under observation in the clinical record

Related Conditions & MeSH terms

• Aging Well

Intervention

Dietary Supplement:
• A power supplement
A dietary supplement containing vitamins and collagen

Locations

Country	Name	City	State
Brazil	Medcin Instituto da Pele	Osasco	São Paulo

Sponsors (2)

Lead Sponsor	Collaborator
Farmoquimica S.A.	Medcin Instituto da Pele Ltda

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Acceptability in real conditions of use by questionnaire	Evaluate the effectiveness of the investigational product (nutritional supplement) in improving signs of facial and body aging, through clinical, instrumental and subjective evaluations. Confirm in real conditions of use, the absence of risk and irritation and capture feelings of discomfort in the population studied (0 meaning no risk)	90 days
Secondary	Evaluation of skin firmness and elasticity using instrumental evaluation - Cutometer	Evaluate the efficacy of the investigational product in improving the firmness and elasticity of the skin through clinical and instrumental evaluations (cutometry) before using the product (D0) and after 45 (D45) and 90 (D90) days of continuous use;	Day 0, Day 45 e Day 90
Secondary	Increase of skin hydration using instrumental evaluation - Corneometer	Evaluate the hydration efficacy before using the investigational product D(0) and after 45 (D45) and 90 (D90) days of continuous use through the Corneometer equipment®	Day 0, Day 45 e Day 90
Secondary	Detection and accuracy of fine lines and wrinkles- Visia	Evaluate the efficacy of the investigational product in improving wrinkles through instrumental evaluations by Visia® before product use (D0) and after 45 (D45) and 90 (D90) days of use continuous	Day 0, Day 45 e Day 90
Secondary	Increase in dermal thickness and density in the thigh region	Check the increase in dermal thickness and density in the thigh region through Ultrasound Volunson E8 before using the product (D0) and after 90 (D90) days of continuous	Day 0 e Day 90
Secondary	Subjective efficacy from the participants	Evaluate the perceived efficacy of the product from the participant's point of view through a subjective questionnaire after 45 (D45) e 90 (D90) days of continuous use of the product	Day 45 e Day 90
Secondary	Acceptability in real conditions of use through dermatological questionnaire	Check the absence of risk of irritation and capture sensations of discomfort from the studied population, through dermatological evaluation criteria.	Day 0, Day 45 e Day 90