Analgesia after Infiltration at the removal site of the graft of the flexor tendons in Anterior Cruciate Ligament Reconstructio
Not Applicable
- Conditions
- Acute painC26.558.554.213
- Registration Number
- RBR-2g3hpyc
- Lead Sponsor
- Clínica de Traumato-Ortopedia do Hospital Naval Marcílio Dias
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Participants who underwent Anterior Cruciate Reconstruction ACL reconstruction with grafts from the flexor tendons; of both sexes; aged between 18 and 50 years will be included
Exclusion Criteria
Patients submitted to revision of Anterior Cruciate Ligament ACL reconstruction, Anterior Cruciate Ligament ACL reconstruction using other grafts; submitted to multiligamentous reconstruction; valgus osteotomy of the tibia or concomitant cartilage repair procedure; allergy to any of the drugs; in chronic use of analgesics; with Body Mass Index BMI above 35 kg/m2 and patients with a history of previous knee surgery
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method it is expected to find a decrease in postoperative pain with the association of adjuvant drugs with local anesthetics by a difference of at least two points based on the method of evaluation of the visual analogue pain scale in the initial 24 hours of surgery in the hospital environment and in the next 6 days in the extra-hospital environment.
- Secondary Outcome Measures
Name Time Method It is expected to find a lower consumption of opioids by the method of evaluating the consumption in grams in the medical prescription of the drug in the hospital and extra-hospital environment.;It is expected to find a better range of motion after 24 hours of surgery and 7 days after surgery using the method of evaluating passive knee extension and flexion using a goniometer measuring degrees.