Trial Information
Inclusion Criteria:
1. Adults above age of 20
2. Undergoing lumbar sympathetic ganglion block indication
Exclusion Criteria:
1. Infection
2. Bleeding tendency
3. Previous spinal surgery history
4. Pregnancy
5. Illiteracy
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
Outcome Measure:
temperature change
Outcome Time Frame:
30min
Safety Issue:
No
Principal Investigator
Jong Bum Choi
Investigator Role:
Study Director
Investigator Affiliation:
Yonsei University
Authority:
Korea: Food and Drug Administration
Study ID:
3-2012-0042
NCT ID:
NCT01648543
Start Date:
June 2012
Completion Date:
December 2012
Related Keywords:
- Lumbar Sympathetic Ganglion Block Indication: Neuropathic Pain, CRPS, Hyperhydrosis Etc.
- Synovial Cyst
- Ganglion Cysts
- Hyperhidrosis
- Neuralgia