Evaluation of clinical efficacy and Perceived Improvement of fatigue in the legs and feet

Medcin Instituto da Pele0 个研究点开始时间: 2015年5月14日最近更新: 2023年5月29日

适应症

试验速览

暂无简介。

•Volunteer female; aged 35-65 years with a history of Chronic Venous Insufficiency; with complaints of episodes of edema, fatigue and heaviness in the legs and feet, agreement to abide by the procedures of the trial and attend the clinic in the days and schedules
•determined for the application and readings and Signing the consent form

•Pregnant; lactating or planning to become pregnant during the study period; use of the following drugs of topical or systemic use immunosuppressants, antihistamines, NSAIDs, and corticosteroids within 30 days before the selection or considering
•immunosuppressants, the interval should be 3 months before screening; atopic or allergic to cosmetics history; pathologies and / or active skin lesions in the area of review (local and or / disseminated); skin marks in the experimental area that interfere with evaluation of possible skin reactions
•(vascular malformations, scars, increasing hairiness, nevus aplenty, sunburn); diseases which cause immune suppression, such as diabetes, HIV;
•endocrine disorders such as thyroid, ovarian or adrenal gland disorders; volunteers with congenital or acquired immunodeficiency known; relevant medical history or current evidence of alcohol or other drugs;
•History known or suspected intolerance to products of the same category; intense sun exposure up to 15 days before evaluation; or dermatological aesthetic treatment in the assessment area up to 04 weeks before screening;
•professionals directly involved in the study design; other conditions considered by the medical examiner as reasonable for disqualification from participation in the study

发起方

Medcin Instituto da Pele