Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05680857
Other study ID # UMRAMREC005-22
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2022
Est. completion date October 30, 2023

Study information

Verified date November 2023
Source Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a placebo-controlled study conducted to investigates the safety and efficacy of products containing marine collagen peptide and CoQ10 in enhancing skin rejuvenation of Malaysian women. The study duration is 28 days and the skin assessment will be carried out at baseline, Day 14 and Day 28.The main questions it aims to answer are: 1. The effect of product on skin hydration of women in Malaysia. 2. The effect of product on skin elasticity of women in Malaysia. 3. The effect of product on skin wrinkle of women in Malaysia. 4. The skin brightening effect of product on Malaysian women. 5. To observe any adverse effect occurrence with the consumption of the product.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date October 30, 2023
Est. primary completion date July 11, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 35 Years to 45 Years
Eligibility Inclusion Criteria: - Malaysian citizen - Women aged 35 - 45 years old - Willing to participate Exclusion Criteria: - Women with skin diseases or any underlying diseases. - Pregnant, breastfeeding women or planned pregnancy during the study period - Allergy to collagen or other ingredients that may be found in the product. - Women who had any cosmetic procedures such as botox, laser and light treatment, facial surgery, and any procedures that may improve skin hydration, elasticity, wrinkles, and brightening of skin four weeks before the study. - Women who took any dietary supplements, functional foods, or medicines that could have the same or similar effects as the product evaluated in this study in the past three months.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Placebo
Product doesn't have active ingredients i.e. marine collagen peptide and Coenzyme Q10.
Product containing marine collagen peptide and Coenzyme Q10.
Product containing marine collagen peptide and Coenzyme Q10.

Locations

Country Name City State
Malaysia Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre Petaling Jaya Selangor

Sponsors (1)

Lead Sponsor Collaborator
Ungku Shahrin Medical Aesthetic Research & Innovation (USMARI) Centre

Country where clinical trial is conducted

Malaysia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in skin hydration from baseline and at Day 14 and Day 28 after consumption of a product. Skin hydration will be assessed using JANUS III skin analyzer and comparison will be made with placebo group. Baseline, Day 14 and Day 28
Primary Changes in skin elasticity from baseline and at Day 14 and Day 28 after consumption of a product. Skin elasticity will be assessed using JANUS III skin analyzer comparison will be made with placebo group. Baseline, Day 14 and Day 28
Primary Changes in skin wrinkles from baseline and at Day 14 and Day 28 after consumption of a product. Skin wrinkles will be assessed using JANUS III skin analyzer comparison will be made with placebo group. Baseline, Day 14 and Day 28
Primary Changes in skin tone from baseline and at Day 14 and Day 28 after consumption of a product. Skin hydration will be assessed using JANUS III skin analyzer comparison will be made with placebo group. Baseline, Day 14 and Day 28
Primary Adverse effect after consumption of product containing marine collagen peptide and coenzyme Q10. Based on adverse effect occurrence on participants that occur during study period (28 days) 28 Days
See also
  Status Clinical Trial Phase
Recruiting NCT06052553 - A Study of TopSpin360 Training Device N/A
Completed NCT05511077 - Biomarkers of Oat Product Intake: The BiOAT Marker Study N/A
Recruiting NCT04632485 - Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
Completed NCT05931237 - Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults N/A
Terminated NCT04556032 - Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women N/A
Completed NCT04527718 - Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers Phase 1
Completed NCT04107441 - AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects Phase 1
Completed NCT04065295 - A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225 Phase 1
Completed NCT04998695 - Health Effects of Consuming Olive Pomace Oil N/A
Completed NCT01442831 - Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects Phase 1
Terminated NCT05934942 - A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood Phase 1
Recruiting NCT05525845 - Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI N/A
Completed NCT05515328 - A Study in Healthy Men to Test How BI 685509 is Processed in the Body Phase 1
Completed NCT04967157 - Cognitive Effects of Citicoline on Attention in Healthy Men and Women N/A
Completed NCT05030857 - Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects Phase 1
Recruiting NCT04714294 - Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers Phase 1
Recruiting NCT04494269 - A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls Phase 1
Completed NCT04539756 - Writing Activities and Emotions N/A
Recruiting NCT04098510 - Concentration of MitoQ in Human Skeletal Muscle N/A
Completed NCT03308110 - Bioavailability and Food Effect Study of Two Formulations of PF-06650833 Phase 1