Overview

Comparison of Different Doses of Dexmedetomidine Effect in the Duration of Spinal Anesthesia

Status:
Unknown status
Trial end date:
2017-07-30
Target enrollment:
0
Participant gender:
All
Summary
Small doses of dexmedetomidine1.5,3, 5µg used in combination with bupivacaine, in humans for spinal anesthesia has been shown to produce a more rapid onset of motor block, and a longer duration of motor and sensory block with preserved hemodynamic stability and lack of sedation.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Cairo University
Treatments:
Dexmedetomidine
Levobupivacaine
Criteria
Inclusion Criteria:

- Patients' physical status by the American Association of Anesthesiology (ASA): ASA I,
II, III, undergoing Lower abdominal surgeries of maximum duration 2hrs

Exclusion Criteria:

- patients who refuse regional anesthesia or patient with bleeding tendency, taking α2-
adrenergic agonist, labile hypertension, uncontrolled cardiac disease, heart
block/dysrhythmia, difficulty in communication e.g. mental retardation or deafness,
body weight more than 120kg or height less than 150cm, allergic to any of the drugs
used in the study