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
| Type | Name | Description |
|---|---|---|
| DRUG | Dexmedetomidine | Dexmedetomidine infusion before intrathecal injection of heavy bupivacaine |
| DRUG | Dexmedetomidine with heavy bupivacaine | Dexmedetomidine 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.