Thoracic vs Lumbar Spinal Anesthesia for Cesarean Delivery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorAdiyaman University Research Hospital

About this trial

This randomized controlled trial aims to compare the effects of thoracic segmental spinal anesthesia and conventional lumbar spinal anesthesia on postoperative recovery in patients undergoing elective cesarean section. Postoperative recovery will be assessed using the ObsQoR-11 score. Hemodynamic parameters, vasopressor and anticholinergic requirements, perioperative complications, and mobilization time will also be evaluated.

Eligibility criteria

Qualifiers

Pregnant women scheduled for elective cesarean section

ASA II-III

Age 18-45 years

Disqualifiers

Contraindications to spinal anesthesia

Coagulopathy or anticoagulant use

Infection at puncture site

Severe cardiac disease

Trial design

Treatments tested in this trial

  • Thoracic Segmental Spinal Anesthesia
  • Lumbar Spinal Anesthesia

Treatment groups

50 Participants
are divided into 2 treatment groups