CTRI/2023/08/056456已完成Unknown
A monocentric, interventional, open label clinical study to evaluate the safety and efficacy of test product (TLS-SA23) on healthy female subjects - NI
Transformative Learning Solutions Pvt Ltd0 个研究点目标入组 38 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 38
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. Each subject with mild to moderate acne and with oily/ acne prone skin (based on lesion count)
- •2. Each subject with oily acne prone skin, sebum casual level on forehead > 90µg/cm2 (mean)
- •3. Subjects having acne based on IGA Scale.
- •4. Subjects having spots, PIH/uneven skin tone and enlarged pores
- •5. Subjects with other skin concern like blemishes, rashes etc.
- •6. Subject free of excessive hair, acne, cuts, abrasions, fissures, wounds, lacerations, or any other active skin conditions on the face.
- •7. Subject who agrees not to use any other product/treatment/home remedy/except the provided products on their face during the study period other than the test product.
- •8.Subjects who agree not to carry out bleaching or any other procedures including facial etc. on face during the study period.
- •9.Subjects who agree not to expose to excessive sun light. (Sun exposure not more than half an hour daily and during that time use of umbrella to cover face).
- •10.Subjects willing to give a voluntary written informed consent, photography release and agree to come for regular follow-up.
- •11. Subjects willing to abide by and comply with the study protocol.
- •12. Subject to agree to remove all jewellery on/around face (e.g., necklace, earrings, if possible, nose ring), during VISIA imaging.
排除标准
- •1. Subjects having cystic acne.
- •2. Subjects with known skin condition that may impact the assessment.
- •3. Subject with any other signs of significant local irritation or skin disease.
- •4. Subject currently taking any medication, which the Investigator believes may influence the interpretation of the data.
- •5. Subject having clinically significant systemic or cutaneous disease, chronic illness or had major surgery in the last year.
- •6. Subjects who do not agree to remove all jewelry on/around face (e.g., necklace, earrings, if possible, nose ring), during Digital imaging.
- •7. Subjects having hair style which covers almost the entire forehead
- •8. Subjects undergoing any treatment of any skin condition on their face.
- •9. Subjects not willing to discontinue other topical facial products.
- •10. Subject allergic or sensitive to bar cleansing products, cosmetics, creams/lotions, artificial jewelry or anything else.
- •11. Pregnant women (as confirmed by UPT) and lactating women
- •12. Subjects on any medical treatment either systemic/topical in the past 1 month or currently taking medication including food supplements.
- •13. Subjects with skin allergy history or atopic dermatitis or psoriasis.
- •14. Subjects who have participated in any other clinical trial in the last 3 months.
- •15. Subjects who were treated with Botox/filler /bio stimulatory molecules injection
研究者
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