Hyperbaric Bupivacaine and Hyperbaric Levobupivacaine in C/S
Information source: Balikesir University
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Health Care; Drugs
Intervention: Hyperbaric levobupivacaine (Drug); Hyperbaric bupivacaine % 0.5 (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: Balikesir University Overall contact: Ozlem Sagir, md, Phone: 00902666121454, Email: ozlemsagir@yahoo.com
Summary
Aim of the Study To compare the effects of hyperbaric bupivacaine plus fentanyl with
hyperbaric levobupivacaine plus fentanyl on spinal block quality, haemodynamics and need
for analgesics in patients undergoing elective cesarean section. Our hypothesis is that
hyperbaric levobupivacaine will provide equal block quality, but better haemodynamic
conditions compared to hyperbaric bupivacaine.
Clinical Details
Official title: The Comparison of Hyperbaric Bupivacaine Plus Fentanyl and Hyperbaric Levobupivacaine Plus Fentanyl Administered Intrathecally in Patients Undergoing Elective Cesarean Section
Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: evaluation of the changes in mean arterial blood pressure between two groups.
Secondary outcome: Time to reach T4 dermatome
Detailed description:
Material - Method 60 patients, American Society of Anesthesiology (ASA) group I-II, between
the ages of 18-45 who were scheduled for elective cesarian section under regional anesthesia
are going to be included. Patients with contraindications to regional anesthesia, known
allergy, suffering from pregnancy induced hypertension or placenta previa will be excluded
from the study.
Patients will not be premedicated. After routine monitorization , IV access and fluid
replacement patients will be separated to two groups on a randomised manner. Under sterile
conditions spinal anesthesia will be performed in the sitting position at the level L3-4 or
L 4-5 via epidural-spinal combined including a 27 G spinal needle.
Group 1 will receive 8 mg hyperbaric bupivacaine plus 20 mcg fentanyl /2ml intrathecally.
Group 2 will receive 8 mg hyperbaric levobupivacaine plus 20 mcg fentanyl/2ml intrathecally.
The Hyperbaric form of Levobupivacaine is not available on market , so it will be prepared
with the addition of % 30 dextrose by another anesthesiologist who will be blinded to the
patients.
Preparation: 2 ml of %0,75 levobupivacaine + 0,8 mL %30 dextrose + 0,2 mL of saline will
be mixed. So it will contain 5 mg levobupivacaine and %8 dextrose per ml.
Hypotension will be defined as a decrease in blood pressure more than % 30 percent of the
basal measured systolic arterial pressure. Hypotension will be treated with 250 ml fast
saline infusion and if no response with 5 mg of ephedrine IV. A heart rate under 50
beats/min will be defined as bradycardia and will be treated with 0. 5 mg atropine i. v.. If
the anesthesia is not sufficient 10 ml of % 0. 25 levobupivacaine wil be administered through
the epidural catheter. The level of sensory and motor block will be evaluated and recorded
every 3 minutes at the beginning and after 15 minutes it will be checked every 5 minutes
until the end of surgery. Maximum level of sensory block, time to reach T4 dermatome and
time to regression of 2 segments will be recorded. Nausea-vomiting, pruritus and shivering
will also be recorded. Baby delivery time, which will be defined as the time from spinal
medication to clamping of the umbilical cord will also be recorded. Total time of surgery
will also be recorded. The time for the first analgesic requirement will be noticed as well.
Patient and surgeon satisfaction will also be evaluated.
Eligibility
Minimum age: 18 Years.
Maximum age: 45 Years.
Gender(s): Female.
Criteria:
Inclusion Criteria:
elective cesarean section no other coexisting medical situation
Exclusion Criteria:
known contraindication to regional anesthesia coexisting pregnancy induced problem
placental mislocation known allergy
Locations and Contacts
Ozlem Sagir, md, Phone: 00902666121454, Email: ozlemsagir@yahoo.com
Balıkesir University Faculty of Medicine, Balıkesir 10145, Turkey; Recruiting Ozlem Sagir, Phone: 00902666121454, Email: ozlemsagir@yahoo.com Ozlem Sagir, MD, Principal Investigator
Additional Information
Starting date: August 2013
Last updated: December 31, 2013
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