ClinicalTrial Intelligence
🏠 Home
📊 Reports
🤖 AI Reports
LOGIN
Login
Sign up
Ensaios Clínicos (somente visualização)
Listagem completa dos ensaios clínicos importados do XML ICTRP.
Back
Id:
473
Trial ID:
RBR-893zqw
Public Title:
Evaluation of improvement of fatigue in the legs and feet
Scientific Title:
Evaluation of clinical efficacy and Perceived Improvement of fatigue in the legs and feet
Scientific Title Native:
None
Recruitment Status:
Data analysis completed
Study Type:
Intervention
Study Design:
n/a, single-arm-study, open
Study Phase:
N/A
Allocation:
None
Masking:
None
Purpose:
None
Date Registration:
2015-05-14
Date Enrolment:
2012-12-03
Last Refreshed:
None
Source Register:
None
Primary Sponsor:
Medcin Instituto da Pele
Secondary Sponsors:
Farmoquimica S.A
Web Address:
https://ensaiosclinicos.gov.br/rg/RBR-893zqw
Target Size:
None
Inclusion Criteria:
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
Exclusion Criteria:
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
Health Conditions:
None
Interventions Summary:
None
Contacts Summary:
None
Results:
None
Countries:
Updated On:
2026-06-01 05:16:50