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Efficacy Testing of VeCollal Products

NCT05789368 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2023-11-09

No results posted yet for this study

Summary

To assess VeCollal formula on skin condition improvement

Conditions

  • Skin Condition

Interventions

DIETARY_SUPPLEMENT

Placebo sachet

consume 1 sachet per day

DIETARY_SUPPLEMENT

VeCollal sachet

consume 1 sachet per day

DIETARY_SUPPLEMENT

Collagen sachet

consume 1 sachet per day

Sponsors & Collaborators

  • TCI Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • Chia-Hua Liang · Chia Nan University of Pharmacy ＆ Science

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-02-06
Primary Completion
2023-04-30
Completion
2023-06-28

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05789368 on ClinicalTrials.gov