Trials / Unknown
UnknownNCT02646501
Prospective Randomized Clinical Trial for Effect of Stellate Ganglion Block in Medically Refractory Ventricular Tachycardia
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- Sponsor
- Yonsei University · Academic / Other
- Sex
- All
- Age
- 20 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
The investigators will compare the effects of PSGB(percutaneous stellate ganglion block) in patients with recurrent sustained VT/VF in spite of appropriate medical therapy and cardio-version/ defibrillation after correction of underlying correctable factors with those without PSGB by prospective randomized trail. PSGB will be performed every 3 days by anesthesiology specialist after cardiologist's request, until the stabilization of VT/VF. We will compare the frequency and episode number of VT/VF, procedure related complication, acute and long-term mortality.
Detailed description
Recurrent ventricular tachycardia(VT)/ fibrillation(VF) increases mortality, especially in patients with structural heart disease. It has been reported that cardiac sympathectomy reduces VT/VF episodes in patients with complex VT, long QT syndrome, catecholaminergic polymorphic VT, or myocarditis. However, cardiac sympathectomy operation is hard to conduct in patients with hemodynamically unstable recurrent VT/VF or electrical storm. Therefore, we hypothesized that bed-side percutaneous stellate ganglion block (PSGB) reduces VT/VF episodes and mortality in patients with repetitive VT/VF who are properly managed with optimal medical therapies.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Antiarrhythmic drug | Antiarrhythmic drug |
| PROCEDURE | percutaneous stellate ganglion block (PSGB) | percutaneous stellate ganglion block (PSGB) |
Timeline
- Start date
- 2019-03-01
- Primary completion
- 2019-09-01
- Completion
- 2019-09-01
- First posted
- 2016-01-05
- Last updated
- 2019-02-11
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT02646501. Inclusion in this directory is not an endorsement.