A Prospective Study of EUS Guided Celiac Block
Completed
- Conditions
- Pancreatic CancerChronic Pancreatitis
- Interventions
- Registration Number
- NCT00583271
- Lead Sponsor
- Indiana University
- Brief Summary
The purpose of this prospective study is to measure the clinical effectiveness of EUS-guided CB in subjects, 50 who have chronic pancreatitis and 50 who have pancreatic cancer, that are already undergoing celiac block for clinical reasons.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 127
Inclusion Criteria
- Patients with chronic abdominal pain from documented chronic pancreatitis or pancreatic cancer or other visceral malignancy that are undergoing EUS-guided CB (for purposes other than this study) will be eligible to participate in this study.
- Patients with chronic pancreatitis and pancreatic cancer must have documented disease by CT, ERCP, or EUS.
- No evidence of dementia or altered mental status that would prohibit the giving and understanding of informed consent, and no evidence of psychiatric risk that would preclude adequate compliance with this protocol.
- Patient must provide signed written informed consent
Exclusion Criteria
- Patients that have had a previous celiac plexus block are eligible for this study
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description 2 98% dehydrated alcohol subjects who are getting a celiac block for pancreatic cancer 1 triamcinolone subjects who are getting a celiac block for chronic pancreatitis
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Clarian Health: Indiana University Hospital
🇺🇸Indianapolis, Indiana, United States