cruciate ligament surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. patients who underwent knee arthroscopic cruciate ligament reconstruction under general anaesthesia with endotracheal intubation; 2. aged 18-64 years; 3. postoperative analgesia by fascia iliaca compartment block catheter; 4. complete clinical history, signs, and examinations; 5. understanding, voluntary participation in the study, signing of the informed consent form, and the ability to communicate fluently.
Exclusion criteria
Exclusion criteria: 1. patients who underwent bilateral knee arthroscopy or other surgical treatments at the same time; 2. patients who were allergy to the drugs related to this study; 3. suffering from severe diabetes mellitus; 4. having neuromuscular disorders in the affected limbs with abnormal muscle strength or sensation before the operation, which affects the clinical assessment; 5. special population groups such as pregnant women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postoperative pain scoring at rest and on movement; | — |
Secondary
| Measure | Time frame |
|---|---|
| Nerve block status (lateral femoral cutaneous nerve, femoral nerve, obturator nerve);Walking on crutches;Flexibility angle of joints;Anesthesia and surgery factors;Dose of anesthetics;fluid Infusion dose; | — |
Countries
China
Contacts
Shantou central hospital