Clinical Trials Directory

Trials / Completed

CompletedNCT02155010

Dexmedetomidine in Spinal Anesthesia

Hemodynamic Effect of Dexmedetomidine on Heavy Bupivacaine Spinal Anesthesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
74 (actual)
Sponsor
Inje University · Academic / Other
Sex
All
Age
20 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Patients were randomized into two groups, A group and B group. A group and B group patients are injected intravenous dexmedetomidine after intrathecal injection (IT) of heavy bupivacaine and injected intravenous dexmedetomidine before IT of heavy bupivacaine, respectively. The investigators will compare of hemodynamics and patient's comfortability between two groups.

Detailed description

A and B group patients will intravenous inject dexmedetomidine 1mcg/kg for 10 minute loading infusion and 0.2mcg/kg/hr for continuous infusion. A group receive intravenous dexmedetomidine after procedure, and B group receive intravenous dexmedetomidine before procedure. Both group patients will hydrate 6 ml/kg crystalloid solution and will evaluated patient's anxiety and comfortability perioperative period. Vital signs will record 5 minutes interval at operating room and post-anesthetic care units.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineDexmedetomidine infusion before intrathecal injection of heavy bupivacaine
DRUGDexmedetomidine with heavy bupivacaineDexmedetomidine infusion after IT of heavy bupivacaine

Timeline

Start date
2014-03-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2014-06-04
Last updated
2016-09-26
Results posted
2016-09-26

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02155010. Inclusion in this directory is not an endorsement.