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Ensaios Clínicos (somente visualização)
Listagem completa dos ensaios clínicos importados do XML ICTRP.
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Id:
464
Trial ID:
RBR-2skhs4
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:
4, single-arm-study, open
Study Phase:
4
Allocation:
None
Masking:
None
Purpose:
None
Date Registration:
2015-05-08
Date Enrolment:
2013-01-21
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-2skhs4
Target Size:
None
Inclusion Criteria:
Pregnancy between 12th and 30th week 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:
Use of the following medications 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; active skin conditions in the assessment area; skin marks in the experimental area that interfere with evaluation of possible skin reactions (vascular malformations, scars, increased hairiness, nevus aplenty, sunburn; pathologies that cause immune suppression, such as diabetes, HIV, endocrine diseases such as thyroid, ovarian or adrenal gland disorders; volunteers with known congenital or acquired immunodeficiency, relevant medical history or current evidence of alcohol or other drugs; known historical or suspected intolerance to products of the same category; intense sun exposure until 15 days before evaluation; aesthetic or dermatologic treatment in the assessment area up to 04 weeks before screening; professionals directly involved in the study design; other conditions considered by the evaluator as reasonable for medical 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