CTRI/2023/06/053922已完成2 期
A clinical study to evaluate the efficacy of the test products in improving hair growth & hair fall reduction.
Hindustan Unilever Ltd0 个研究点目标入组 216 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 216
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. Male and female volunteers in general good health with mild to moderate hair fall
- •2. Volunteers in the age group 18-50 years (both the ages inclusive).
- •3. Volunteers willing to give a written informed consent and agree to come for a regular follow up visit.
- •4. Volunteers willing to abide by and comply with the study protocol.
- •5. Volunteers who have not participated in a similar investigation in the past three months.
- •6. Volunteers with no known allergy as established by medical history.
- •7. Volunteers who do not smoke or drink alcohol.
- •8. Volunteers who are not crash dieting.
- •9. Volunteers who agree to refrain from using hair dye / hair colour during the study period.
- •10. Volunteers willing to refrain from any type of hair treatment like perming, straightening etc. during the study duration.
- •11. Volunteers who are willing to refrain from any other oil treatment/hair spa and oral medications for hair growth during the study.
排除标准
- •1. Volunteers who have undergone hair growth treatment within 3 months before screening into the study.
- •2. Volunteers having any active scalp disease which may interfere in the study dermatologist’s judgement.
- •3. Volunteers who have taken chemotherapy for cancer in the 6 months prior to start of the study or have a plan to do treatments during study.
- •4. Volunteers who have history of alcoholism and/ or psychiatric disorder including trichotillomania.
- •5. Volunteers who have had hair transplants.
- •6. Volunteers who take pharmaceutical product which cause hirsutism (ex. phenytoin) and finesteride for androgenic alopecia.
- •7. A known history or present condition of allergic response/hypersensitivity to any cosmetic ingredients and pharmaceutical products.
- •8. Volunteers consuming alcohol and smoking
- •9. Volunteers on oral medications which will compromise the study.
- •10. Volunteers who are pregnant or lactating or nursing as established with medical history.
- •11. Volunteers under any medical treatment for hair problems
- •12. Undergoing any chemical hair salon treatment-straightening / perming / colour
- •13. Menopausal female volunteers as determined by medical history.
- •14. Pregnant and lactating female volunteers
- •15. Chronic illness which may influence the cutaneous state. Volunteers participating in other similar cosmetic or therapeutic trial within last three months.
- •16. Any history of underlying uncontrolled medical illness including diabetes mellitus, hypertension, HIV, hepatitis, severe anemia, serious disorder of heart and respiratory apparatus or any other serious medical illness.
研究者
相似试验
已完成
不适用
A clinical study for evaluating the efficacy of the highly-concentrated oxygen nanobubble water -immune function, fatigue, autonomic nervous function and skin functionJPRN-UMIN000018755Soiken Inc.17
尚未招募
3 期
Shirishadi Malhar & Parushakadi Yog in the Management of KIKKISA w.s.r. to STRIAE GRAVIDARUMCTRI/2023/07/055029Government of Himachal Pradesh
已完成
不适用
A clinical study for evaluating the efficacy of test food on the suppression of the elevation of postprandial blood glucose level. -Randomised double-blind placebo-controlled trialHealthy adultJPRN-UMIN000035336KSO Corporation50
已完成
不适用
A clinical study for evaluating the efficacy of test food on the suppression of the elevation of postprandial blood glucose levelHealthy adultJPRN-UMIN000043321Pharma Foods International Co., Ltd.30
已完成
不适用
A clinical study for evaluating the efficacy of test food on the suppression of the elevation of postprandial serum triglyceride. : Randomised double-blind placebo-controlled trialHealthy adultJPRN-UMIN000036241Allegro Inc.30