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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: REBEC
Last refreshed on: 29 April 2013
Main ID:  RBR-32ym5t
Date of registration: 25/09/2011
Primary sponsor: Universidade de Brasília - Brazil
Public title: Electrical stimulation in healthy individuals
Scientific title: Interferencial current produce peripheral vasodilation in healthy individuals - INTER: Interferential
Date of first enrolment: 01/01/2010
Target sample size: 11
Recruitment status: data analysis completed
URL:  http://www.ensaiosclinicos.gov.br/rg/RBR-32ym5t/
Study type: 
Study design:  Clinical Trial, randomized, blinded with four arms  
Countries of recruitment
Brazil
Contacts
Name: Francisco   Santos
Address:  Rua Napoleão de Barros, 715, 3º andar 04023-002 São Paulo Brazil
Telephone: 11-82335019
Email: valdezs@terra.com.br
Affiliation:  Universidade Federal de São Paulo
Name: Francisco   Santos
Address:  Rua Napoleão de Barros, 715, 3º andar 04023-002 São Paulo Brazil
Telephone: 11-82335019
Email: valdezs@terra.com.br
Affiliation:  Universidade Federal de São Paulo
Key inclusion & exclusion criteria
Inclusion criteria: Individuals of both sexes, with age group from 19 to 44 years, non-smokers, non-obese and free of any signs or symptoms of disease, as revealed by the medical history, physical examination and electrocardiogram at rest and during exercise
Exclusion criteria: Pregnancy, breastfeeding, alcohol or drug abuse and any medication with potential effects on the circulation

Age minimum: 19Y
Age maximum: 44Y
Gender: -
Health Condition(s) or Problem(s) studied
Study in healthy subjects
A08.800.050
Intervention(s)
There were two pairs of electrodes placed in the C7 and T4 levels. Interferential current was applied in mid-frequency for a period of 45 minutes, with current fixed frequency of 4000 Hz and AMF in 25 Hz, with intensity set at sensory level, without causing pain or muscle contraction.Each subject underwent the intervention twice on different days. Four groups were established: Interferential Current + Handgrip with Post Exercise Circulatory Occlusion (PECO); Interferential + Handgrip without PECO; Control + Handgrip with PECO; and Control + Handgrip without PECO.
Primary Outcome(s)
Calf blood flow (Units) and Calf vascular resistance (ml.min-1.100g-1)
Measurement of variables using venous occlusion plethysmography (TL 400, Hokanson, Bellevue, United States)
Calf blood flow and Calf vascular resistance
Secondary Outcome(s)
HR was measured using a monitor (Polar, Kempele, Florida, United States) and MAP was measured in the non-dominant arm using a calibrated oscillometric automatic device (Dinamap Model 1846SX / P, Critikon, Tampa, Florida, United States)
Mean Blood Pressure (MBP) and Heart rate (HR)
Secondary ID(s)
253/2009
Source(s) of Monetary Support
Universidade Federal de São Paulo - Brazil
Secondary Sponsor(s)
Hospital das Clinicas de Porto Alegre - Brazil
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