CTRI/2023/04/051262尚未招募Unknown
Efficacy Evaluation Of Cosmetic Formulations In Conferring Skin Pore Constricting Benefits in Healthy Human Participants.
ITC Life Sciences Technology Centre0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Participants in the age group of 19 to 50 years
- •2· Participants with enlarged skin pores, varied skin types including Sensitive skin
- •3· Participants willing to abide by the study protocol and refrain from using any product other than the provided Investigational product during the study course.
- •4· Participants with varied skin type i.e., normal, dry, oily, combination and sensitive skin in nearly equal ratio.
- •5· Participants willing to visit the site for periodic assessments on the scheduled dates.
- •6· Participants who exhibits good tolerance to the investigational product with no signs of sensitivity.
- •7· Participants who agree to refrain from any other test product during the study
- •8· Participants willing to give voluntary written informed consent and photography release.
- •9· Participants willing to abide by and comply with the study protocol.
- •10· Participants able to read and sign an appropriate informed consent form indicating their willingness to participate.
- •11· Participants willing and capable to follow the study rules and a fixed schedule.
排除标准
- •1. Pregnant or lactating women
- •2· Participants undergoing treatment for Seborrhoea, Acne, Dermatitis, skin lightening/ any other cosmetic/ dermatologic skin condition on face
- •3· Participants with pre-existing systemic disease requiring long-term medication (self-declaration)
- •4· Participants with genetic and endocrinal disorders [ self-disclosure]
- •5· Participants with drug induced acne [ self-disclosure]
- •6· Participants with any other signs of significant local irritation or skin disease.
- •7· Participants on oral hormonal treatment or oral medications (e.g., steroids, anti-oxidant) for eight weeks prior to the study which will compromise the study.
- •8· Participants who may change personal nutrition habits and other habits as per investigatorâ??s discretion.
- •9· Participants who have participated in a similar investigation or any other clinical product evaluation test in the past four weeks
- •10· Participants under the influence of alcohol and/or drugs as well as addiction.
- •11· Participants with severe psychological illness or intellectual inability to understand the study.
- •12· Participants who have wounds, sunburn, scars, tattoos or piercings at the skin test sites.
- •13· Participants with uncontrolled disease (severe heart/circulatory, liver, kidney or lung disease, severe diabetes mellitus) or chronic infections (hepatitis, HIV)
- •14· Participants who have proven allergies against cosmetic ingredients or prior intolerance responses after applying cosmetic products.[ self-disclosure]
- •15· Participants who are taking antihistamines and/or medication to suppress the immune system (e.g., corticoids, cytostatics) and/or retinoids
- •16· Participants who might participate in any other clinical study during participation in the current study
- •17· Participants currently taking any medication, which the investigator believes may influence the interpretation of the data.
- •18· Participants having chronic or acute skin disease at the skin test sites within the last 14 days prior to the beginning of the study and/or during the study or had major surgery in the last year.
- •19· Participants undergoing any treatment of any active skin condition
- •20· Participants allergic or sensitive to bar cleansing products, creams/lotions, artificial jewellery or anything else.
- •21· Participants who are pregnant or nursing.
研究者
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