Effects of Oral and Topical Sea Buckthorn Oil Treatments on Skin Aging (SBanti-aging)

Subjective and Instrumental Evaluation of the Effects of Treatments With Two Sea Buckthorn Oil Products on Cutaneous Aging

The effect of oral supplementation of SBA24 sea buckthorn oil capsule and topical application of Omega7 sea buckthorn cream on skin ageing is studied in a single blind, parallel study.

Study Overview

• Status: Unknown
• Conditions: Skin Aging
• Intervention / Treatment: Dietary supplement: SBA24 Sea Buckthorn Oil Capsule; Dietary supplement: SBA24 Sea Buckthorn Oil Capsule; Other: Omega7 Sea Buckthorn Oil Cream; Other: Base cream

Detailed Description

The study is carried out on two groups of female volunteers, 30 in each group, of age 30 to 60 years, in compliance with the principles established by the World Medical Association in the Declaration of Helsinki. In group I, the subjects took SBA24 sea buckthorn oil capsule (2 x 2 capsules per day) and apply two different creams on the face, one cream on each half of the face, twice per day. In group II, the subjects apply only the two creams, one cream on each half of the face, twice per day, for 8 weeks.

The assessment is performed on the skin surface of the periocular areas.

The efficacy of the active products is assessed on the skin face at the beginning, after 4 weeks and after 8 weeks of treatment using the following instrumental measurements:

• cutaneous elasticity (CUTOMETER SEM 575 Courage & Khazaka);
• cutaneous hydration level (CORNEOMETER CM 825 Combi 3 Courage & Khazaka);
• cutaneous roughness by cutaneous replicas and image analysis (Quantilines, Monaderm); Determination of benefit is based on instrumental measurements and subject self-assessment questionnaires.

• Study Type: Interventional
• Enrollment (Anticipated): 60
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Italy
  • Milan, Italy, 20125
    • ISPE Srl

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 26 years to 56 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

• Female subjects 30 - 60 years old with Fitzpatrick skin type I-IV & in good general health, with facial skin manifestation related to photoaging (wrinkles, dyschromias, tissue looseness etc.)
• Subjects must have discontinued the use of topical retinoid products for 6 months prior to study entry and of systemic retinoids for 1 year prior to study entry.
• Subjects must have discontinued the use of topical alpha-hydroxy, &/or beta-hydroxy products for 45 days prior to study entry & all other topical facial medication to the skin immediately prior to study entry.
• Subjects must have discontinued the use of systemic antiaging or antioxidant products for at least 2 months prior to study entry.
• Subjects must be willing & able to follow all study directions & to commit to all follow-up visits for the duration of the study.
• Subjects must have completed the informed consent process.
• Subjects must be willing to avoid direct daily sun exposure on the face or the use of tanning beds.

Exclusion Criteria:

• Pregnant or nursing females.
• Subjects with a history of unusual skin reactions to skin care toiletry products, cosmetics, or sensitivity to any of the test article components.
• Previous facial treatments with any dermal fillers (i.e. collagen, hyaluronic acid etc)
• Concurrent therapy, systemic diseases, or skin disorders (such as eczema, psoriasis, severe acne etc.) which may interfere with the evaluation of the test articles or increase risk to the subject.
• Subjects currently involved in another clinical investigation or who have been involved within a period of 30 days prior to admission in this study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: SBA24 capsule plus Omega7 cream; the subjects took SBA24 sea buckthorn oil capsule and apply Omega7 cream	Dietary supplement: SBA24 Sea Buckthorn Oil Capsule; The subjects take SBA24 sea Buckthorn Oil Capsules, 2 x 2 capsules (2.0 g oil) per day and use topically Omega7 Sea Buckthorn Oil Cream, twice per day.; Other Names: Omega7/Membrasin Capsule, Omega7 Cream; Dietary supplement: SBA24 Sea Buckthorn Oil Capsule; Teh subjects took SBA24 Sea Buckthorn Oil Capsule, 2 x 2 capsules (2 g oil) per day and use topically the base cream, twice per day; Other Names: Omega7/Membrasin/SBA24 Sea Buckthorn Oil Capsule
Active Comparator: SBA24 capsule plus base cream; the subjects took SBA24 sea buckthorn oil capsule and apply a base cream	Dietary supplement: SBA24 Sea Buckthorn Oil Capsule; The subjects take SBA24 sea Buckthorn Oil Capsules, 2 x 2 capsules (2.0 g oil) per day and use topically Omega7 Sea Buckthorn Oil Cream, twice per day.; Other Names: Omega7/Membrasin Capsule, Omega7 Cream; Dietary supplement: SBA24 Sea Buckthorn Oil Capsule; Teh subjects took SBA24 Sea Buckthorn Oil Capsule, 2 x 2 capsules (2 g oil) per day and use topically the base cream, twice per day; Other Names: Omega7/Membrasin/SBA24 Sea Buckthorn Oil Capsule
Active Comparator: Omega7 Cream; The subjects Omega 7 Sea Buckthorn Oil Cream, twice per day	Other: Omega7 Sea Buckthorn Oil Cream; The subjects use Omega7 Sea Buckthorn Oil Cream on the face, twice per day
Placebo Comparator: Base cream; The subjects use base cream on the face, twice per day	Other: Base cream; The subjects use the base cream on the face, twice per day

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Decrease of signs of skin aging	8 weeks

Secondary Outcome Measures

Outcome Measure	Time Frame
Subjects self-assessment of the efficacy of the treatment	8 weeks

Collaborators and Investigators

• Sponsor: Institute of Skin and Product Evaluation, Italy
• Collaborators: Aromtech Ltd.
• Investigators: Principal Investigator: Adriana Bonfigli, PhD, Research Director

Study record dates

Study Major Dates

• Study Start: October 1, 2008
• Primary Completion (Anticipated): November 1, 2008
• Study Completion (Anticipated): December 1, 2008

Study Registration Dates

• First Submitted: October 3, 2008
• First Submitted That Met QC Criteria: October 3, 2008
• First Posted (Estimate): October 6, 2008

Study Record Updates

• Last Update Posted (Estimate): October 6, 2008
• Last Update Submitted That Met QC Criteria: October 3, 2008
• Last Verified: October 1, 2008

More Information

Terms related to this study

• Keywords: Sea buckthorn oil, Oral and topical treatment, Skin aging
• Other Study ID Numbers: E11UE15UE25US14C