Effect of Intraoperative Ankle Nerve Blocks on Postoperative Discharge in Patients Undergoing Orthopaedic Foot Surgery
Operative Incision
About this trial
This is an interventional diagnostic trial for Operative Incision focused on measuring Ankle nerve block, post operative analgesia, patient satisfaction, foot surgery
Eligibility Criteria
Inclusion Criteria:
- Patient's acceptance,
- American Society of Anesthesiologists physical status I-III
- elective orthopedic foot surgery
- general anesthesia
Exclusion Criteria:
- Pregnancy
- history of chronic pain therapy
- hypersensitivity to study drugs
- allergy to study drugs
- blood coagulation disorder
- anticoagulant use
Sites / Locations
- University of Health Dıskapı Yıldırım Beyazıt Training and Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Group General Anesthesia
Group Ankle Block
These group patients will be monitored with ECG, pulse oximetry and noninvasive blood pressure. Anesthesia will be induced using 2-2.5 mg/kg propofol, 1-2 mcg/kg fentanyl, 10 mg-20 mg rocuronium and a proper size laryngeal mask airway will be placed to secure the airway. The lungs will be ventilated with a mixture of 50% and 50% oxygen.
These group patients will be monitored with ECG, pulse oximetry and noninvasive blood pressure. Anesthesia will be induced using 2-2.5 mg/kg propofol, 1-2 mcg/kg fentanyl, 10 mg-20 mg rocuronium and a proper size laryngeal mask airway will be placed to secure the airway. The lungs will be ventilated with a mixture of 50% and 50% oxygen. After than an ankle block will be performed in patient group block patients using a mixture of 5 ml of 2% lidocaine and 10 ml of 0.5 bupivacaine the same amount placebo (saline) in group placebo under the guidance of peripheral nerve stimulator then the anesthesia will be disconnected and LMA will be removed. The patients will be transferred from postoperative care unit toward after they are eligible for discharge according to the modified scoring system.