Overview

Comparing the Effects of Levobupivacaine and Bupivacaine in Saddle Spinal Anesthesia

Status:
Completed
Trial end date:
2008-12-17
Target enrollment:
0
Participant gender:
All
Summary
İn this study; it was aimed to investigate the effects of equipotent doses of hyperbaric bupivacaine and hyperbaric levobupivacaine in outpatient anorectal surgery under saddle block. Sixty patients between the age of 18- 50 and in the risk group of ASA I-II included in the study. 7,5 mg of 0,5% hyperbaric bupivacaine or 7,5 mg of 0,5% hyperbaric levobupivacaine injected into the intrathecal space in sitting position through L4-L5 or L5-S1 intervertebral space in 30 seconds. All patients kept in sitting position for 5 minutes with aid after intrathecal injection and than layed in supine position, finally they positioned in prone jack-knife. Hemodynamic parameters like NIBP, HR, SpO2, sensory and motor block characteristics, duration of analgesia, time of first voiding, mobilization time, patient and surgeon satisfaction, adverse effects and discharge time were recorded during and after surgery.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Gazi University
Treatments:
Bupivacaine
Levobupivacaine
Criteria
Inclusion Criteria:

- ASA I-II risk group with planned elective anorectal surgery

- Approved to participate in the study and spinal anesthesia

Exclusion Criteria:

- Known hypersensitivity to amid-type local anesthetics

- Not to accept regional anesthesia administration

- With preoperative motor and sensory loss

- Not to accept participation in the study

- Contraindications for spinal anesthesia method