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Comparison of the Cosmetic Effects of Bakuchiol and Retinol

University of California (UC) Davis logo

University of California (UC) Davis

Status and phase

Completed
Early Phase 1

Conditions

Photoaging
Wrinkle

Treatments

Drug: Bakuchiol
Drug: Retinol

Study type

Interventional

Funder types

Other

Identifiers

NCT03112863
1015536

Details and patient eligibility

About

Subjects will be assigned to a retinoid cream or bakuchiol to compare the cosmetic effects. This will take place over a 12 week period.

Full description

Bakuchiol is a phytochemical that has demonstrated cutaneous antiageing effects when applied topically. Early studies have suggested that bakuchiol is a functional analogue of topical retinoids, as both compounds have been shown to induce similar gene expression in the skin and lead to improvement of cutaneous photodamage. No in vivo studies have compared the two compounds for efficacy and side-effects.

The aim of this study is to compare the cosmetic effects of Bakuchiol to Retinol over a 12-week period.

Enrollment

44 patients

Sex

All

Ages

30 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

• Individuals aged 30-55

Exclusion criteria

  • Adults unable to consent
  • Individuals who are not yet adults (infants, children, teenagers)
  • Pregnant or breast feeding women
  • Prisoners
  • Those with acne, eczema, seborrheic dermatitis, rosacea or polycystic ovarian syndrome
  • Those who have used isotretinoin in the last 6 months
  • Those who have used products containing salicylic acid, beta hydroxyl acids or vitamins A, C, or E in the last 14 days
  • Those who have used topical antibiotics or topical retinoids in the last 30 days
  • Those who are currently smoking or have smoked within the past 3 years.
  • Those who have had a recent surgical or cosmetic procedure in the last 3 months that can affect facial wrinkles or facial hyperpigmentation, such as botulinum toxin injections, chemical peels, laser based therapies to the face, or face lift surgeries

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

44 participants in 2 patient groups

Bakuchiol
Experimental group
Description:
Bakuchiol 0.5% applied to face twice daily
Treatment:
Drug: Bakuchiol
Retinol
Active Comparator group
Description:
0.5% retinol applied to face nightly
Treatment:
Drug: Retinol

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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