Modified Saddle Block vs Spinal Anesthesia for TURP
Sponsor: Pakistan Institute of Medical Sciences • ClinicalTrials.gov ID: NCT07841184
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After obtaining informed consent, eligible patients will be enrolled in the study. Standard monitoring will be applied in the operating room and baseline blood pressure and heart rate will be recorded. Participants will be randomly assigned to receive either spinal anesthesia or a modified saddle block using hyperbaric bupivacaine administered in the lower back. The position of the patient after injection will differ according to the assigned anesthetic technique. The level of numbness produced by the anesthesia will be assessed, and patients with inadequate anesthesia will be excluded. Blood pressure and heart rate will be monitored regularly during surgery. Any significant decrease in blood pressure will be treated with intravenous phenylephrine. Any need to change to general anesthesia during the procedure will also be recorded.
Interventions
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Saddle block
(Drug)
Patients will receive with 15 mg of hyperbaric bupivacaine at L3 L4 level using 25 G spinal needle and will be made to sit for 5 minutes before lying down
-
Spinal Anesthesia (bupivacaine)
(Drug)
Patients will receive spinal anesthesia with 15mg of hyperbaric bupivacaine at L3 L4 level using 25G spinal needle and will be immediately made to lie down
Eligibility criteria
Conditions
Locations
- Deparmtent of Anesthesia and Critical Care Medicine, Pakistan Institute of Medical Sciences — Islamabad, Federal, Pakistan
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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