About this trial
Spinal anesthesia is a commonly employed technique for lower abdominal surgeries, providing effective anesthesia and analgesia with minimal systemic effects. In cancer patients undergoing such procedures, careful consideration of anesthetic techniques is crucial, given their often-compromised physiological state and the need to minimize postoperative complications. Two approaches to administering spinal anesthesia are Ultrasound (US)-guided and the traditional landmark-based technique.
the aim of the study :To evaluate the efficacy, safety and feasibility of US-guided spinal anesthesia versus the landmark-based technique in cancer patients undergoing lower abdominal surgery.
Eligibility criteria
Qualifiers
Age >18 years old
Both sex
patients with a body mass index (BMI) of 18-40 kg/m2
American Society of Anesthesiologists (ASA) physical status classification of I to III.
Disqualifiers
• Patients have a contraindication for regional anesthesia, e.g. coagulopathy.
Failed or unsatisfactory intrathecal block.
Patients with known hypersensitivity to amide local anesthetics.
Local injection site infection or spinal deformity.
Trial design
Treatments tested in this trial
- spinal anesthesia
- spinal anesthesia