NCT00583271CompletedNot Applicable
A Prospective Study of Endoscopic Ultrasound-guided Celiac (CB) Effectiveness
Conditions
Interventions
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Indiana University
- Enrollment
- 127
- Locations
- 1
Study Overview
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.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
Arms & Interventions
2
subjects who are getting a celiac block for pancreatic cancer
Intervention: 98% dehydrated alcohol (Drug)
1
subjects who are getting a celiac block for chronic pancreatitis
Intervention: triamcinolone (Drug)
Investigators
Study Sites (1)
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