Evaluation of the Skin-Beautifying Effects of Collagen Drinks
NCT ID: NCT06900660
Last Updated: 2025-03-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
NA
30 participants
INTERVENTIONAL
2025-01-13
2025-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Efficacy Evaluation of Collagen Drink Products
NCT06194487
Efficacy Testing of Collagen Drink on Skin Beauty and Sleep Aid
NCT05182814
Efficacy Evaluation of Avance QQ Collagen for Skin Beautification
NCT06771388
Assessment of Anti-aging Efficacy of Marine Collagen Peptides
NCT06306105
Effect of Oral Collagen Tripeptide on Skin Moisture and Wrinkles in Adult Women
NCT03505684
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
OTHER
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Collagen Drinks
The Collagen Drinks contain collagen peptides and antioxidants
Collagen Drinks
Dosage: 50 mL/day; duration: 8 weeks
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Collagen Drinks
Dosage: 50 mL/day; duration: 8 weeks
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Healthy people
Exclusion Criteria
2. Pregnant and lactating women
3. Hypersensitivity to the assigned product
4. Diagnosed with skin diseases, liver diseases, kinedy disease, and other severe diseases
5. Cosmetic, drug, or food allergies
6. Concurrent aesthetic treatments (e.g., intense pulse light, medical peelings, or laser therapy)
7. Aceepted aesthetic treatments one month ago before the study
8. Chronic sun exposure (over 3 hours/day)
9. The members of the research team
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Chia Nan University of Pharmacy ＆ Science
OTHER
Simply Plus Co., Ltd.
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Chia-Hua Liang
Role: PRINCIPAL_INVESTIGATOR
Department of Cosmetic Science, Chia Nan University of Pharmacy ＆ Science
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Chia Nan University of Pharmacy ＆ Science
Tainan City, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
25-007-B
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.