NCT05724589

Brief Summary

EGF is a polypeptide that promotes cell differentiation and collagen production while decreasing melanin production. This study is designed to study its effectiveness in improving the texture and appearance of facial skin after daily topical application. We hypothesized that EGF would improve facial skin hydration, elasticity, pigmentation, and wrinkles.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
28

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 30, 2023

Completed
Same day until next milestone

Study Start

First participant enrolled

January 30, 2023

Completed
14 days until next milestone

First Posted

Study publicly available on registry

February 13, 2023

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 5, 2024

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 12, 2024

Completed
8 months until next milestone

Results Posted

Study results publicly available

July 31, 2025

Completed
Last Updated

July 31, 2025

Status Verified

July 1, 2025

Enrollment Period

1.3 years

First QC Date

January 30, 2023

Results QC Date

January 11, 2024

Last Update Submit

July 14, 2025

Conditions

Outcome Measures

Primary Outcomes (6)

  • Facial Skin Hydration

    Facial skin hydration was measured using a Corneometer, which provides readings in arbitrary units (a.u.). Measurements were taken at baseline (Day 0), Week 8, Week 12, and Week 16 under standardized environmental and procedural conditions to ensure reliability and accuracy. Higher values indicate better skin hydration, while lower values indicate increased dryness.

    4 months (Baseline, Week 8, Week 12, Week 16)

  • Transepidermal Water Loss

    measured by tewameter on day 0, then at 8, 12, and 16 weeks.

    4 months

  • Facial Skin Elasticity (R2 Parameter Via Cutometer)

    Skin elasticity was assessed using a Cutometer with the R2 parameter (Ua/Uf), which measures gross elasticity. R2 values range from 0 to 1.0, with higher values indicating better skin elasticity. Measurements were collected under standardized conditions at Baseline (Day 0), Week 8, Week 12, and Week 16.

    Baseline, Week 8, Week 12, Week 16

  • Facial Skin Wrinkles

    Visioscan measurements were taken at baseline, then at 8, 12, and 16 weeks by using a 4-grade percentage wrinkle improvement scale.

    4 months

  • Facial Melanin Index

    Facial pigmentation was assessed using the Mexameter, which measures melanin content via light absorption and reflection. The device reports values on a scale from 0 to 999, where higher values represent greater melanin concentration. Measurements were collected at standardized facial sites at Baseline, Week 8, Week 12, and Week 16. Higher scores indicate worse pigmentation.

    4 months

  • Overall Facial Skin Appearance (Photo Evaluation Using SGAIS)

    Facial skin appearance was evaluated using the Subject Global Aesthetic Improvement Scale (SGAIS), a 5-point scale where higher scores indicate greater improvement. Scores were assigned by two board-certified dermatologists who assessed photographs taken by the Visia-CR imaging system at Baseline, Week 8, Week 12, and Week 16. SGAIS scoring definition: 1 = Worse, 2 = Mild improvement (\<25%), 3 = Moderate (25-49%), 4 = Much improved (50-74%), 5 = Very much improved (≥75%).

    4 months

Secondary Outcomes (2)

  • Subject Satisfaction in Improving Skin Hydration, Elasticity, Wrinkles, and Pigmentation

    4 months

  • Adverse Events

    4 months

Study Arms (1)

Epidermal Growth Factor Serum Application

EXPERIMENTAL

Participants received Epidermal growth factor serum application on the face daily for two months compared to pre and post-results of skin quality.

Drug: Epidermal Growth Factor

Interventions

Apply facial twice daily.

Also known as: Epidermal Growth Factor Serum
Epidermal Growth Factor Serum Application

Eligibility Criteria

Age40 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Thai
  • Mild to moderate facial skin condition, as measured by 1-2 points on the hyperpigmentation status scale or 2-3 points on the wrinkle severity grading scale.

You may not qualify if:

  • Use of lotions or skin care products containing ingredients such as vitamin A/C, hydroquinone, or anti-aging agents.
  • Sunbathing
  • Hypersensitivity to serum components
  • Pregnancy and breast-feeding
  • Active skin diseases such as eczema or atopic dermatitis at the application site

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Institute of Dermatology

Bangkok, 10400, Thailand

Location

MeSH Terms

Interventions

Epidermal Growth Factor

Intervention Hierarchy (Ancestors)

Gastrointestinal HormonesHormonesHormones, Hormone Substitutes, and Hormone AntagonistsEGF Family of ProteinsIntercellular Signaling Peptides and ProteinsPeptidesAmino Acids, Peptides, and ProteinsProteinsBiological Factors

Limitations and Caveats

The small sample size should be considered. Further research involving a larger population or control group is recommended for conclusive insights into the efficacy of EGF serum.

Results Point of Contact

Title
Dr. Supawee Phanmamuang
Organization
Institute of Dermatology, Thailand

Study Officials

  • Chumsaeng Chumsaengsri

    Institute of Dermatology

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident of Dermatology

Study Record Dates

First Submitted

January 30, 2023

First Posted

February 13, 2023

Study Start

January 30, 2023

Primary Completion

June 5, 2024

Study Completion

December 12, 2024

Last Updated

July 31, 2025

Results First Posted

July 31, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations