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Nutritional Study of Fish Oil in Skin Quality in Healthy Women (OPTIHUD)

E

Epax

Status

Unknown

Conditions

Skin Health

Treatments

Dietary Supplement: Ceto 10
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT05128240
P237921

Details and patient eligibility

About

The skin acts as a barrier against the external environment and prevents water loss from the body. Aging is a natural process leading to changes in the skin and fish oil has been shown to prevent inflammation, hyperpigmentation and UV-damage. This pilot study will determine skin characteristics after intervention with north atlantic fish oil.

Full description

Women will be recruited to a placebo or fish oil group and be examined at pre- and post for skin quality parameters such as wrinkles, fine lines and trans-epithelial water loss.

Enrollment

30 estimated patients

Sex

Female

Ages

30 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy women in the age of 30-65

Able to follow the following dietary restriction for 4 months (4 weeks wash-out, 3 months intervention):

  • Do not take omega-3 supplements
  • do not take supplements containing vitamin A
  • do not take supplements containing collagen
  • try to avoid using skin products containing vitamin A
  • do not undergo skin treatment

Exclusion criteria

Pregnancy or breast feeding known allergy to seafood skin treatment the last 6 months planned skin treatment during the study period

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

30 participants in 2 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
4x1g corn oil capsules
Treatment:
Dietary Supplement: Placebo
Ceto 10
Experimental group
Description:
4x1g capsules containing containing broad spectrum marine oil from north atlantic fish
Treatment:
Dietary Supplement: Ceto 10

Trial contacts and locations

1

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Central trial contact

Derek Tobin, PhD

Data sourced from clinicaltrials.gov

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