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Lasertherapy and electrical stimulation on Lateral Epicondylitis: joint function and tendon repair.

Photobiomodulation and diadynamic currents on Lateral Epicondylitis: joint function and tissue repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5zb4dg
Enrollment
Unknown
Registered
2018-09-26
Start date
2018-10-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lateral Epicondylitis

Interventions

The volunteers will be distributed randomly in 3 groups: group 1 (GFBM), Photobiomodulation and exercise protocol
group 2 (GE), electrical stimulation and exercise protocol
group 3 (GC), exercise protocol. Each group will have 22 volunteers. All groups will receive the proposed treatment for 8 weeks, performing 2 sessions per week. The 3 groups will be submitted to the s
Device
E02.331
E02.774

Sponsors

Universidade Federal de São Paulo
Lead Sponsor
Universidade Estadual de Campinas
Collaborator

Eligibility

Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Volunteers will be included if they meet the following criteria: age between 18 and 70 years; less than 6 months of epicondylalgia symptoms; absence of systemic diseases; pain at palpation over the lateral epicondyle region of the elbow or common tendon pathway of the extensor muscles; pain to the movement of wrist extension against resistance Visual Analog Scale (AVE) score of pain equal to or greater than 3 and diagnosis of lateral epicondylitis of the elbow.

Exclusion criteria

Exclusion criteria: Will be excluded from the study volunteers who present a history of fracture in the elbow joint; carriers of osteosynthesis metal material in the upper limb; patients with cardiac pacemakers; tactile sensory deficit in the upper limb; history of conservative or surgical treatment for epicondylalgia in the last 3 months; use of anti-inflammatory medication during the experiment and volunteers who underwent corticosteroid injection in the last 3 months.

Design outcomes

Primary

MeasureTime frame
Improvement of function for the manual activities, resulting from the applied treatment, evaluated by the Patient-rated Tennis Elbow Evaluation (PRTEE), verifying the reduction of at least 11 points in the questionnaire to consider the significative result.

Secondary

MeasureTime frame
Reduction in the level of pain at rest with the proposed treatment, verified by a numerical scale of the pain of 11 points (0 to 10), considering a reduction of at least 3 points as a significant improvement.

Countries

Brazil

Contacts

Public ContactRicardo Guerra

Universidade Estadual de Campinas

rsguerra@unicamp.br+55-19-35218999

Outcome results

None listed

Source: REBEC (via WHO ICTRP)