NCT07793123

Brief Summary

A randomized, double-blind, placebo-controlled study evaluating the effects of an oral antioxidant dietary supplement on skin radiance in women exposed to urban air pollution. Secondary assessments include skin tone homogeneity, pigmentation, inflammation, skin barrier function, glycation markers.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

July 31, 2026

Completed
28 days until next milestone

First Posted

Study publicly available on registry

August 28, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Expected
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

August 28, 2026

Status Verified

July 1, 2026

Enrollment Period

3 months

First QC Date

July 31, 2026

Last Update Submit

August 25, 2026

Conditions

Keywords

SkinpollutionRadiance

Outcome Measures

Primary Outcomes (1)

  • Skin Radiance

    Glossymeter

    Day 0 and Day 90

Secondary Outcomes (7)

  • Skin Radiance

    Day 0 and Day 30

  • Skin Radiance

    Day 0, Day 30, Day 90

  • Skin homogeneity

    Day 0, Day 30, Day 90

  • Skin homogeneity

    Day 0, Day 30, Day 90

  • TransEpidermal Water Loss

    Day 0, Day 30, Day 90

  • +2 more secondary outcomes

Study Arms (2)

Dietary supplement : Placebo

PLACEBO COMPARATOR

Maltodextrin = 400 mg/capsule, 1 capsule per day.

Dietary Supplement: Placebo

Dietary supplement : Investigational product

ACTIVE COMPARATOR

1 capsule contains :140 mg Rosa damascena extract, 20 mg melon concentrate and 140 mg acerola extract; 57mg maltodextrin; 1 capsule per day.

Dietary Supplement: Antioxidant Supplement

Interventions

Antioxidant SupplementDIETARY_SUPPLEMENT

Oral antioxidant dietary supplement administered as one capsule once daily for 90 days.

Dietary supplement : Investigational product
PlaceboDIETARY_SUPPLEMENT

Placebo dietary supplement administered as one capsule once daily for 90 days.

Dietary supplement : Placebo

Eligibility Criteria

Age35 Years - 65 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Healthy female aged 35 to 65 years
  • Fitzpatrick skin phototype II to IV
  • All skin types
  • Dull and uneven skin tone
  • Living in an urban environment and exposed to air pollution
  • Able to comply with study procedures
  • Written informed consent provided

You may not qualify if:

  • Pregnant or breastfeeding
  • Current use of dietary supplements or vitamin supplements
  • Specific dietary restrictions
  • Unstable medication affecting water retention
  • Active medical disease
  • Facial dermatological disorder
  • Participation in another clinical trial
  • Vulnerable populations according to French regulations

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gredeco

Paris, 75 013, France

Location

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 31, 2026

First Posted

August 28, 2026

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

August 28, 2026

Record last verified: 2026-07

Locations