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A Prospective Study of EUS Guided Celiac Block

Indiana University logo

Indiana University

Status

Completed

Conditions

Chronic Pancreatitis
Pancreatic Cancer

Treatments

Drug: 98% dehydrated alcohol
Drug: triamcinolone

Study type

Observational

Funder types

Other

Identifiers

NCT00583271
0205-04B
IRB #0205-04B

Details and patient eligibility

About

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.

Enrollment

127 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

127 participants in 2 patient groups

1
Description:
subjects who are getting a celiac block for chronic pancreatitis
Treatment:
Drug: triamcinolone
2
Description:
subjects who are getting a celiac block for pancreatic cancer
Treatment:
Drug: 98% dehydrated alcohol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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