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临床试验/NCT05842447
NCT05842447已完成不适用

Effect of Two Doses of Pomanox® Pomegranate Extract Consumption on Skin Ageing. Randomized, Parallel, Placebo Controlled and Triple Blind Clinical Trial (POMASKIN).

Fundació Eurecat4 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2023年10月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
66
试验地点
4
主要终点
Change in skin melanin index.

研究概览

简要总结

The state of skin health impacts not only on the general health of individuals, but also on mental health. Ultraviolet radiation (UV) is one of the main external factors that causes skin ageing, producing photo-aging, characterized by multiple alterations in the skin such as the appearance of wrinkles, dryness, erythema, alterations in the pigmentation, inflammation and increased fragility.

Several studies show that polyphenols extracts, including pomegranate extracts, have beneficial effects on various skin characteristics induced by photoaging by modulating internal factors that lead to changes associated with photoaging. Among these internal factors are oxidative stress, glycation stress caused by an accumulation of advances glycation end-products (AGEs), inflammation, and the composition of the intestinal and skin microbiota.

Pomanox® is a polyphenolic extract derived from pomegranate for which antioxidant activity and positive effects on the metabolism of collagen and hyaluronic acid have been shown in previous in vitro studies.

详细描述

The hypothesis of the study is that the consumption of Pomanox®P30 will have beneficial effects on skin ageing in humans through the modulation of the metabolism of collagen, hyaluronic acid and the inflammatory system, the inhibition of the production of reactive oxygen species and AGEs, and/or changes in the intestinal and skin microbiota composition.

The main objective of the study is to evaluate the effect of consuming two doses of Pomanox®P30 on hyperpigmented skin spots in humans.

The secondary objectives of the study are to evaluate the effects of consuming two doses of Pomanox®P30 on other parameters related to skin ageing (wrinkles, elasticity, erythema index, hydration, pores, acne and keratin), on different markers of collagen and hyaluronic acid metabolism, oxidative stress, the anti-glycan effect and the inflammatory system, and on the composition of the intestinal and skin microbiota.

A randomized, parallel, placebo-controlled, single-center, triple-blind clinical trial with a 1:1:1 ratio between interventions with 66 participants will be conducted.

Each participant will make 4 visits:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
30 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Women aged 30 years or older and 65 years or less.
  • Fitzpatrick skin phototype II-IV.
  • Read, write and speak Catalan or Spanish.
  • Sign the informed consent.

排除标准

  • Present any chronic gastrointestinal disease that may interfere with the objectives of the study such as celiac disease, Crohn's disease, ulcerative colitis, irritable bowel syndrome with symptoms in the last 6 months, chronic diarrhea, or having undergone any bariatric surgery procedure.
  • Present a chronic disease with clinical manifestation and/or being under pharmacological treatment that may interfere with participation in the study.
  • Present values of body mass index ≥ 35 kg/m^
  • Present a clinical history of active anemia.
  • Have consumed or intended to consume during the study treatments, supplements or multivitamin supplements or phytotherapeutic products that interfere with the study treatment (such as retinol or vitamin A, vitamin C, vitamin E, antioxidants, polyphenols, probiotics and prebiotics) up to 30 days before the start of the study intervention.
  • Have consumed or intended to consume during the study contraceptive treatments or hormonal therapy up to 30 days before the start of the study intervention.
  • Have taken treatment with antibiotics up to 30 days before the start of the study intervention.
  • Have taken or intended to take treatments for acne, for photo-ageing or to improve the appearance or condition of the skin (such as chemical peeling, laser therapy, light therapy or hyaluronic acid injection; regular treatment in a facial beauty salon, skin whitening agents) up to 6 months before the start of the study intervention.
  • Being a smoker or ex-smoker in the last 6 months before inclusion in the study.
  • Consume 2 o more Standard Beverage Units daily or 17 weekly.
  • Present allergy and/or intolerance to the study products (such as presenting hypersensitivity to maltodextrin or allergy to pomegranate).
  • Being pregnant or intending to become pregnant.
  • Being in breastfeeding period.
  • Being participating, intending to participate or having participated in a clinical trial or nutritional intervention study in the last 30 days before inclusion in the study.
  • Present any skin disease (such as atopic skin, eczema, neurodermatitis, vitiligo or psoriasis) or any skin disorder in the sudy area (such as irritations, moles, scars or macules).
  • Have been intensely exposed to the sun or artificial ultraviolet radiations (solarium) in the test area during the 30 days before the start of the study or planning to do so during the study.
  • Not being able to follow the guidelines of the study.

结局指标

主要结局

Change in skin melanin index.

时间窗: At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).

Skin melanin index measured by using a Mexameter® MX18.

次要结局

  • Change in Human Procollagen I C-Terminal Propeptide blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in Metalloproteinase-1 blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in hyaluronic acid blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in superoxide dismutase activity blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in reduced gluthathione blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in pentosidine blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in skin wrinkles.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in skin hydratation.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in skin elasticity.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in skin erythema index.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in skin pores.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in skin acne.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in skin keratin.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in Human Procollagen I N-Terminal Propeptide blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in carboxymethyl-lysine blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in interleukin-1 alpha blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in interleukin-6 blood levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in stool microbiota composition.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in skin microbiota composition.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in dimethylellagic acid glucuronide urine levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Change in urolithin A glucuronide urine levels.(At day 1 (visit V1) and day 85 (visit 3).)
  • Subject self-assessment quality of the skin.(At day 29 (visit V2) and day 85 (visit 3).)
  • Age.(At day -7 (pre-selection visit).)
  • Height.(At day -7 (pre-selection visit).)
  • Change in body weight.(At day -7 (pre-selection visit), day 1 (visit V1, day 29 (visit 2) and day 85 (visit 3).)
  • Change in body mass index.(At day -7 (pre-selection visit), day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in fat mass.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Change in muscle mass.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Concomitant medication.(At day -7 (pre-selection visit), day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Dietary supplements consumed.(At day -7 (pre-selection visit), day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Use of cosmetic treatments.(At day -7 (pre-selection visit), day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Exposure to ultraviolet radiation.(At day -7 (pre-selection visit), day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Products with pomegranate and ellagitannins consumption.(At day -7 (pre-selection visit), day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Eating habits.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Physical activity.(At day 1 (visit V1), day 29 (visit 2) and day 85 (visit 3).)
  • Intervention compliance.(At day 29 (visit 2) and day 85 (visit 3).)
  • Adverse events.(At day 29 (visit 2) and day 85 (visit 3).)

研究者

发起方
Fundació Eurecat
申办方类型
Other
责任方
Principal Investigator
主要研究者

Antoni Caimari

Director of Eurecat's Biotechnology Area

Fundació Eurecat

研究点 (4)

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