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Evaluated the Efficacy and Safety of APCP on Hair Health

NCT06422026 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2024-05-22

No results posted yet for this study

Summary

This study is designed to evaluate the efficacy and safety of APCP in promoting hair health in adult with mild to moderate hair damage, compared to a placebo control.

Conditions

  • Hair Damage

Interventions

DIETARY_SUPPLEMENT

APCP I

Each subject takes one active bottle per day for 24 weeks. Each bottle contains APCP 3 g.

DIETARY_SUPPLEMENT

APCP II

Each subject takes one active bottle per day for 24 weeks. Each bottle contains APCP 4 g.

DIETARY_SUPPLEMENT

Placebo

Each subject takes one active bottle per day for 24 weeks.

Sponsors & Collaborators

  • Amorepacific Corporation

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-03-16
Primary Completion
2024-01-30
Completion
2024-04-30

Countries

  • South Korea

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 NCT06422026 on ClinicalTrials.gov