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Prospective Evaluation of Topical Almond Oil vs Hydroquinone

NCT04875715 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-09-12

No results posted yet for this study

Summary

The purpose of this study is to analyze facial pigmentation and skin microbiome changes after topical almond oil application, compared to the use of topical hydroquinone.

Conditions

  • Skin Pigmentation

Interventions

OTHER

Almond Oil

Almond oil

DRUG

Hydroquinone Topical

Hydroquinone 2% cream

Sponsors & Collaborators

  • University of California, Davis

    lead OTHER

Principal Investigators

  • Raja Sivamani, MD MS AP · UC Davis Dermatology

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-01
Primary Completion
2026-08-01
Completion
2026-08-01
FDA Drug
Yes

Countries

  • United States

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 NCT04875715 on ClinicalTrials.gov