Evaluation of Pain after Knee Surgery using Pregabalin before and after Surgery

Not Applicable

Recruiting

• Conditions: Pain Postoperative; Anterior Cruciate Ligament Injuries; C10.597.617.841; C26.558.554.213

• Registration Number: RBR-7ncggq
• Lead Sponsor: Hospital São Domingos

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-05-30
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Patients diagnosed with chronic knee instability; patients older than 18 years; physical status classification according to the scale of the American Society of Anesthesiologists (ASA) I and II;
without local and systemic inflammatory diseases; isolated lesions of the anterior cruciate ligament (no other knee ligaments);
no history of fractures in the knee region;
absence of previous surgeries in the knee region; operated by the orthopedist of the team;
ability to read, understand and agree to the inclusion of your data
in this research.

Exclusion Criteria

Skeletally immature patients; chondral lesions greater than 2 cm2; associated surgical procedures, such as osteotomies, and other knee ligaments; neurological, muscular, rheumatologic, neoplastic or infectious diseases that could provoke some type of joint involvement (gout, multiple myeloma,
psoriasis, lymphoma, Paget's disease, rheumatoid arthritis, chronic renal failure,
osteomyelitis, ankylosing spondylitis, systemic lupus erythematosus); patients without clinical conditions, hypertensive, with coagulopathies, pregnant women; chronic use of anticoagulants; use of analgesics up to 24 h before the surgical procedure; patients who refused to sign the EHIC; patients not operated at the São Domingos Hospital; refusal or impossibility of the patient to perform the postoperative rehabilitation; non-acceptance of the anesthesiologist in following the protocol of the project; patients allergic to the medications used in the protocol; patients who declared themselves indigenous.

Study & Design

• Study Type: Intervention
• Study Design: Not specified