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Skin Hydration in Persons With Acne After Dietary Supplementation With Botanical Antioxidants (KIWIBOOSTER)

University of California, Los Angeles (UCLA) logo

University of California, Los Angeles (UCLA)

Status

Withdrawn

Conditions

Acne
Acne Vulgaris

Treatments

Dietary Supplement: HBKB Capsule
Other: HBKB Supplement Vehicle

Study type

Interventional

Funder types

Other

Identifiers

NCT04534140
19-002095

Details and patient eligibility

About

Antioxidants have been studied for their abilities to combat reactive oxygen species in a multitude of conditions. This study aims to assess whether the botanical dietary supplement 'Halo Beauty Kiwi Booster' (HBKB), taken orally daily for 8 weeks, can assist with Acne vulgaris as well as skin hydration and quality of life for those with acne.

Full description

The study will be a 2-armed investigational trial with one group receiving botanical dietary supplement and one placebo group provided with the similar supplement vehicle. The trial will be double-blind, randomized, parallel-group study. The investigational group will receive the botanical dietary supplement 'Halo Beauty Kiwi Booster' (HBKB), to be taken orally daily for 8 weeks. Control group participants will receive the HBKB botanical dietary supplement vehicle as a placebo to be taken orally daily for 8 weeks.Participants will have their skin assessed

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults 18-35 years of age able to provide consent to participate
  • IGA of mild to moderately severe facial Acne Vulgaris (AV) at screening
  • Potential participants with mild to moderately severe facial AV and with AV on their neck, shoulders, chest and/or back body surface areas may be included.

Exclusion criteria

  • An Investigator Global Assessment IGA of severe facial, neck, back or truncal AV
  • Diagnosis of a chronic inflammatory disease such as lupus, multiple sclerosis, cancer, Chron's disease or cancer
  • Allergies to Astaxanthin (microalgae), Grape Seed Extract, Kiwi fruit or Kiwi extract, Pineapple fruit or extract (bromelain), Rosehip or Rosehip extract, Gooseberry, Rosehip, Grapes
  • Secondary AV, such as occupational AV, steroid induced AV, or AV associated with endocrine disorders
  • Having facial dermatosis that may interfere evaluations by IGA such as sunburn, eczema, psoriasis, erythematotelangectatic rosacea or seborrheic dermatitis
  • Use of isotretinoin within 2 months
  • Use of adapalene or tretinoin within 2 weeks
  • Use of anti-biotics within 2 weeks
  • Use of oral corticosteroids or androgens within 2 weeks
  • Use of anticonvulsants
  • Any subject who the PI deems unsuitable for any reason

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

0 participants in 2 patient groups, including a placebo group

HBKB Capsule
Experimental group
Description:
Experimental group participants will take one capsule of the HBKB botanical dietary supplement orally, once daily
Treatment:
Dietary Supplement: HBKB Capsule
HBKB Capsule Vehicle
Placebo Comparator group
Description:
Control group participants will take one capsule of the HBKB botanical dietary supplement vehicle orally, once daily
Treatment:
Other: HBKB Supplement Vehicle

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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