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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02688426
Other study ID # LLLT-CABG-2016/1
Secondary ID
Status Recruiting
Phase N/A
First received February 18, 2016
Last updated March 21, 2016
Start date March 2015
Est. completion date June 2016

Study information

Verified date March 2016
Source Federal University of Health Science of Porto Alegre
Contact Rodrigo Plentz, PhD
Phone +55 51 33038835
Email roplentz@yahoo.com.br
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

The low-level laser therapy (LLLT) has been used in many inflammatory disorders.

More recently the LLLT was associated with an improvement in the muscle strength, endurance and functional capacity.But, these effects were described only in health or athletic individuals. In this randomized and controlled clinical trails, the investigators will study the effects of LLLT on functional capacity of the patients with Coronary artery bypass surgery.


Description:

This study will be conducing in a large hospital that is reference in Coronary artery bypass surgery. 15 patients will be randomized for placebo or low-level laser therapy (LLLT). The functional capacity will be test by test six-minute walk test before and after de LLLT. Moreover the application of LBP or placebo will be followed by assessments of muscle damage and oxidative stress. One-week interval between the LLLT will gave to reduce the influence between the treatments.


Recruitment information / eligibility

Status Recruiting
Enrollment 15
Est. completion date June 2016
Est. primary completion date February 2016
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria:

- Patients in the postoperative period of elective CABG referred for cardiac rehabilitation, which are the 15th and 30th days after surgery without ischemic changes and / or complex arrhythmias on the electrocardiogram, between 40 and 75 years of age who have performed the first surgery.

Exclusion Criteria:

- Patients with decompensated heart failure; presence of any comorbidity such as: unstable angina; associated neurological disease; moderate respiratory illness to severe pre-diagnosed by the attending physician; active infectious disease or fever; disabling peripheral vascular disease; unstable ventricular arrhythmias; diabetes mellitus; use of cardiac pacemaker, musculoskeletal disease that limits physical activity, patients with a BMI =30.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Sham Low-Level Laser Therapy (Sham LLLT)
perform with the machine off
6J Low-Level Laser Therapy (6J LLLT)
irradiation will be perform with 6J

Locations

Country Name City State
Brazil Rodrigo Della Méa Plentz Porto Alegre RS

Sponsors (1)

Lead Sponsor Collaborator
Federal University of Health Science of Porto Alegre

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Six-minute walk test up to 2 weeks No
Secondary Muscle damage The damage to DNA is analyzed by electrophoresis single (comet technique), where cells are counted by microscopy. up to 2 weeks No
Secondary Oxidative stress Oxidative stress will be used a measure of tissue damage, the protein oxidation (method of carbonyls) and two defense measures, an enzyme superoxide dismutase and total antioxidant capacity. Oxidative damage (nmol / mg) of protein carbonylation was determined according to the method proposed by Levine & Stadtman, 1990, using whole blood. The enzymatic activity of SOD (SOD / mg protein) was determined by the inhibition of autooxidation of adrenaline measured spectrophotometrically (480nm) under Bannister and Calabrese (1987). up to 2 weeks No
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