Landmark Versus Ultrasongraphy Guided Spinal Anesthesia in Lower Abdominal Surgeries in Cancer Patients: a Randomized Controlled Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssiut University

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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • spinal anesthesia

    Procedure/Surgery

    spinal anesthesia after us-assisted technique

  • spinal anesthesia

    Procedure/Surgery

    spinal anesthesia using the surface landmark-guided

Treatment groups

52 Participants
are divided into 2 treatment groups
Group A: Landmark GroupExperimental treatment 1 intervention
Group B: Ultrasonography GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

the first-pass success rate of Combined spinal-epidural anesthesia

first-pass success was defined as the needle reaching the subarachnoid space within a single insertion attempt, without redirection

Time frame
baseline

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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