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NCT04345094

Evaluation of Hexyresorcinol vs Hydroquinone for Photoaging

Completed NA Last updated 10 July 2020
What this trial tests

NA trial testing Hexylresourcinol in Photoaging in 32 participants. Completed in 15 February 2020.

Timeline
1 July 2019
Primary endpoint
24 December 2019
15 February 2020

Quick facts

Lead sponsorSytheon Ltd.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment32
Start date1 July 2019
Primary completion24 December 2019
Estimated completion15 February 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Sytheon Ltd.

Who can join

Adults 35 to 65, female only, with Photoaging. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Photoaging is a common concern within the cosmeceutical industry with many products that are available. One frequently used product is hydroquinone that is used to even skin tone. However, hydroquinone has several shortcomings. The ingredient is controversial for its potential safety issues and it has been banned in Europe. An alternative ingredient that has emerged for its potential use is hexyresorcinol for evening skin tone. Additionally, hexylresorcinol may have other photoaging benefits such as the reduction in the appearance of fine lines. Therefore, the aim of this study is to assess how hexyresorcinol may compare to the use of hydroquinone in the setting of photoaging.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Prospective, randomized, double-blind clinical study of split-body comparison of topical hydroquinone and hexylresorcinol for skin pigment appearance.
    Wu H, Gabriel TA, Burney WA, Chambers CJ, et al · · 2023 · cited 9× · PMID 36502500 · DOI 10.1007/s00403-022-02514-0

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04345094.

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