Venous ulcer Leg Ulcer
Conditions
Interventions
This is an exploratory, randomized, controlled, double-blind clinical trial with four parallel arms. Participants will be randomly assigned to four groups: a control group (n = 5), receiving conventio
Group 1 (n = 5), receiving conventional treatment combined with low-level laser therapy at an energy of 0.5 J per point
Group 2 (n = 5), receiving conventional treatment combined with low-level laser therapy at an energy of 1 J per point
and Group 3 (n = 5), receiving conventional treatment combined with low-level laser therapy at an energy of 2 J per point, totaling 20 participants. Laser therapy will be administered once a week for
s double-blind design. The randomization sequence will be generated beforehand using a spreadsheet created in Numbers software. Twenty random numbers will be generated using the random function and ar
Sponsors
Universidade Federal de Juiz de Fora
Hospital Universitário da Universidade Federal de Juiz de Fora
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Individuals of both sexes; aged 18 years or older; new patients admitted to wound care outpatient clinics; presence of a lesion of vascular etiology
Exclusion criteria
Exclusion criteria: Prior laser treatment; diagnosis contraindicating the use of low-level laser; cancer; decompensated glaucoma; pregnancy; use of a pacemaker
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the reduction in wound healing time using serial evaluation via the Bates-Jensen Wound Assessment Tool (BWAT) scale and measurement of the wound with a two-dimensional ruler, and from this, to observe if there was a progressive decrease in size and the time required for complete healing | — |
Secondary
| Measure | Time frame |
|---|---|
| To establish a clinical protocol for the treatment of venous lesions based on scientific evidence regarding the efficacy of low-level laser therapy and the optimal power level to be applied, using a comparison between randomized groups through observation of differences in scores on the Bates-Jensen Wound Assessment Tool (BWAT) scale, healing time, and clinical evolution of the lesions;Evaluate the reduction in pain, exudate volume, and dressing change frequency using the Numerical Visual Scale (NVS) to measure pain, assess exudate volume by saturating the primary dressing, and record the need for dressing changes, observing reductions in Bates-Jensen Wound Assessment Tool (BWAT) scores and decreased dressing change frequency | — |
Countries
BR
Contacts
Public ContactCassia Delgado
Universidade Federal de Juiz de Fora
Outcome results
None listed