Study to Investigate the Effect of Superba Boost on the Skin

Trans-epidermal Water Loss Clinical Trial

Official title:

A Randomised, Double-blinded, Parallel, Placebo-controlled Study to Investigate the Effect of Superba Boost (Krill Oil Concentrate) on Various Skin Parameters in Healthy Adult Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05711303
• Other study ID #: AFCRO-097
• Status: Completed
• Phase: N/A
• Start date: March 13, 2019
• Est. completion date: December 20, 2019

Study information

• Verified date: February 2023
• Source: Atlantia Food Clinical Trials
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Study to determine the effect of 12 weeks daily consumption of Superba Boost as compared to placebo on reduction in Trans-Epidermal Water-Loss (TEWL).

Description:

This study is a randomized, double-blind, placebo-controlled, parallel group trial in 70 healthy adult male and female subjects between 20 and 50 years. The primary objective is to assess whether Superba Boost krill oil administered at a dose of 1 g per day for 12 weeks (84 days) has a positive effect on the TEWL, skin hydration and elasticity. At screening, the subjects must have TEWL values of >10 g/m2/h and <24.9 g/m2/h when measured by a TWEAmeter, i.e. within the range defined as normal and healthy skin. The change in omega-3 index, defined as EPA and DHA as percentage of total fatty acids in red blood cells, will be measured and correlated to the changes in the skin parameters. The study consists of 4 visits: the screening visit (V1), baseline visit / week 0 / Start of treatment (V2), Interim / Week 6 (V3) and week 12 / end of treatment (V4) . In this study, subjects must have a low habitual consumption of fatty fish and seafood, defined as a frequency of twice per month or less will be recruited.

Each subject must fulfill all inclusion criteria and will not be allowed to meet any of the exclusion criteria.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: December 20, 2019
• Est. primary completion date: August 12, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 50 Years

Eligibility

Inclusion Criteria:

To be eligible for inclusion, the subject must fulfil all of the following criteria:

1. Be able to give written informed consent;

2. Be aged between 20 and 50 years, inclusive;

3. Trans-epidermal water loss score >10 and = 24.9 g/m²/h;

4. Be in general good health with no existing co-morbidities

5. Have a low habitual consumption of fatty fish and seafood, defined as a frequency of twice per month or less;

6. Be willing to avoid all fish and seafood meals in the 4-days before each scheduled clinic visit;

7. Be willing to maintain dietary habits and physical activity levels throughout the trial period;

8. Be able to communicate well with the Investigator, to understand and comply with the requirements of the study, and be judged suitable for the study in the opinion of the Investigator;

9. Willing & able to consume the investigational product daily for the duration of the study.

Exclusion Criteria:

The presence of any of the following criteria will exclude the subject from participating in the study:

1. Pregnant or breastfeeding women; women planning to become pregnant during the study;

2. Women of child-bearing potential who do not use an acceptable method of contraception;

3. Suffer from photosensitivity;

4. History of skin cancer;

5. Are currently taking photosensitizing medication, or have done so in the previous 4 weeks;

6. Sunbed tanning or sunbathing in preceding 3 months, or planned sunbed tanning or sunbathing during the study period

7. Taking supplements known to have an effect on skin (e.g. fish oil, coenzyme Q-10, garlic, lycopene, beta-carotene, etc.), or have done so in the previous 4 weeks, except for medically-prescribed supplements or natural health products.

8. Supplements known not to have an effect on the skin (e.g. probiotics) are allowed, once the subject has been on a stable dose for greater than 3 months and are willing to continue this supplement for the duration of the study;

9. Systolic blood pressure =160 mmHg, diastolic blood pressure =100 mmHg. Subjects receiving blood pressure medications, must be on stable dose for greater than 3 months;

10. Known allergy to seafood;

11. Are hypersensitive to any of the components of the test product;

12. Disturbed absorption due to changes in the gastrointestinal tract (e.g., resections, diverticula, malabsorption, blind-loop syndrome);

13. Known alcohol abuse (> 21 units of alcohol per week) or drug abuse within the previous year of screening;

14. Clinically significant illness within 14 days prior to dosing;

15. Current or recent (within 3 months of screening visit) changes in diet, which in the opinion of the Investigator, deviates from a normal diet (e.g. vegetarians may be acceptable, vegans are not acceptable);

16. Planned major changes in life style (i.e. diet, dieting, exercise level, travelling) during the duration of the study;

17. Has any health conditions that would prevent from fulfilling the study requirements, put the subject at risk or would confound the interpretation of the study results as judged by the investigator on the basis of medical history and routine laboratory test results;

18. Are severely immunocompromised (HIV positive, transplant patient, on antirejection medications, on a steroid for >30 days, or chemotherapy or radiotherapy within the last year);

19. Experiences alarm features such as weight loss, rectal bleeding, recent change in bowel habit (<3 months) or abdominal pain;

20. Have a malignant disease or any concomitant end-stage organ disease;

21. Individuals who, in the opinion of the investigator, are considered to be poor attendees or unlikely for any reason to be able to comply with the trial;

22. Subjects receiving treatment involving experimental drugs. If the subject has been in a recent experimental trial, these must have been completed not less than 60 days prior to this study.

Related Conditions & MeSH terms

• Trans-epidermal Water Loss

Intervention

Dietary Supplement:
• Superba Boost
To assess changes in Trans-epidermal water loss (TEWL), measured at baseline and after 12 weeks of intervention using a TEWAMetre.

Locations

Country	Name	City	State
Ireland	Atlantia Food Clinical Trials	Cork	Munster

Sponsors (1)

Lead Sponsor	Collaborator
Atlantia Food Clinical Trials

Country where clinical trial is conducted

Ireland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	To determine the effect of Superba Boost versus the placebo on the Lipid content of skin (Exploratory)	Skin content of the following lipids at week 6 and week 12 measured in pmol; Analysis will be performed on the following lipids: Nonhydroxydehydrosphingosine (NdS); Nonhydroxysphingosine (NS); Nonhydroxyphytosphingosine (NP); Nonhydroxy-6-hydroxysphingosine (NH); Alphahydroxydehydrosphingosine (AdS); Alphahydroxysphingosine (AS); Alphahydroxyphytosphingosine (AP); Alphahydroxy-6-hydroxysphingosine (AH); Omegahydroxysphingosine (EOS); Omegahydroxyphytosphingosine (EOP); Omegahydroxy-6-hydroxysphingosine (EOH); Omegahydroxydehydrosphingosine (EOdS); diacylglycerol; free cholesterol; cholesterol esters; triacylglycerols.	12 weeks
Primary	To determine the effect of 12 weeks daily consumption of Superba Boost as compared to placebo on reduction in Trans-Epidermal Water-Loss (TEWL).	Reduction in Trans-epidermal water loss (TEWL), measured at baseline and after 12 weeks of intervention using a TEWAMetre.	12 weeks.
Secondary	To determine the effect of daily consumption of Superba Boost as compared to placebo on the reduction of Trans-epidermal water loss (TEWL),	Changes in Trans-epidermal water loss (TEWL) from baseline to 6 weeks after start of treatment, using a TEWAMetre	6 weeks.
Secondary	To assess the effect of daily consumption of Superba Boost as compared to placebo on changes in skin hydration	Changes in skin hydration from baseline (pre-study) to 6 weeks after start of treatment using a Corneometer	6 week
Secondary	To assess the effect of daily consumption of Superba Boost as compared to placebo on changes in skin hydration	Changes in skin hydration from 6 weeks of treatment until end-of-study using a Corneometer	6 weeks
Secondary	To assess the effect of daily consumption of Superba Boost as compared to placebo on changes in skin firmness (6 weeks)	Changes in skin firmness from baseline (pre-study) to 6 weeks after start of treatment using a Cutometer	6 weeks
Secondary	To assess the effect of daily consumption of Superba Boost as compared to placebo on changes in skin firmness	Changes in skin firmness from 6 weeks of treatment until end-of-study using a Cutometer	6 weeks
Secondary	To assess the effect of daily consumption of Superba Boost as compared to placebo on changes on subjective evaluation	Subjective evaluation by study subjects, using questionnaires at 6 weeks of treatment	6 weeks
Secondary	To assess the effect of daily consumption of Superba Boost as compared to placebo on changes on subjective evaluation	Subjective evaluation by study subjects, using visual analogue scale at 12 weeks of treatment lower scores indicating worse outcomes and higher scores indicating better outcomes.	12 weeks
Secondary	To assess the effect of daily consumption of Superba Boost as compared to placebo on changes on Omega-3 index	Omega-3 index (%), using a blood spot collected by fingerpick	12 weeks