TENS in the postoperative anterior cruciate ligament rupture
Not Applicable
- Conditions
- Knee injuryC26.558.554
- Registration Number
- RBR-9fzfys
- Lead Sponsor
- niversidade Luterana do Brasil
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Subjects aged between 18 and 40 years with ACL rupture who underwent surgery through the bone-tendon-arthroscopic technique admitted to the Santa Luzia hospital; Have signed the Informed Consent Form.
Exclusion Criteria
Prior rupture of meniscus requiring prior repair; Evidence of degenerative disease on radiological imaging or MRI; Patients with deficit of superficial sensitivity; Patients with loss of level of consciousness; Cognitive disability that makes it impossible to understand and sign the consent form to participate in the study; Patients with previous stroke sequelae; Patients who develop wound infection; Death during the research period.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method