Evaluating Predictors & Interventions in Sphincter of Oddi Dysfunction (EPISOD)

This study is ongoing, but not recruiting participants.
Information provided by (Responsible Party):
Peter Cotton, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ClinicalTrials.gov Identifier:
First received: May 30, 2008
Last updated: August 31, 2012
Last verified: August 2012

Protocol Title:Evaluating Predictors & Interventions in Sphincter of Oddi Dysfunction(SOD) Acronym EPISOD

Clinical Trial Phase: Phase III

Study Sites Seven clinical centers in US

Study Period Planned enrollment period - 3 years

Planned duration of the study - 5 years

Study Population SOD III Patients

Primary Study Objective: To ascertain whether subjects with SOD III respond to sphincterotomy,

Secondary Study Objectives

To evaluate:

  • the association between the results of Sphincter of Oddi Manometry (SOM) (abnormal/normal) and the primary outcome (success/failure);
  • the success rate (as defined in the primary) of subjects who receive biliary sphincterotomy alone versus subjects who receive both biliary and pancreatic sphincterotomy in the subgroup of patients with manometrically proven hypertension of the pancreatic sphincter;
  • the effects of pre-specified prognostic factors on the primary outcome;
  • anxiety and depression scores over time and their relation to study outcomes;
  • the economic impact of SOD III, and of endoscopic sphincterotomy in patients with SOD III; and, to,
  • conduct a careful follow-up study (EPISOD2) of standard of care treatment (separate protocol).

Study Design The EPISOD Trial is a two-arm parallel, randomized, double-blinded, sham-controlled, multicenter Phase III clinical trial of endoscopic sphincterotomy as treatment for adults 18 to 65 years of age diagnosed with SOD III.

Sample Size A minimum of 214 subjects will be randomized using a 2:1 allocation in favor of sphincterotomy and will be followed for 12 months post-randomization.

Condition Intervention Phase
Sphincter of Oddi Dysfunction
Procedure: Pancreatic Sphincterotomy
Procedure: Pancreatic and Biliary Sphincterotomy
Procedure: ERCP
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Official Title: A Phase III Randomized Multicenter Clinical Trial of Sphincterotomy for the Treatment of SOD III Patients

Resource links provided by NLM:

Further study details as provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK):

Primary Outcome Measures:
  • To ascertain whether subjects with SOD III respond to sphincterotomy, [ Time Frame: 5 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • the association between the results of Sphincter of Oddi Manometry (SOM) (abnormal/normal) and the primary outcome (success/failure) [ Time Frame: 5 years ] [ Designated as safety issue: No ]

Estimated Enrollment: 214
Study Start Date: July 2008
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
Pancreatic Sphincterotomy
Procedure: Pancreatic Sphincterotomy
cutting the sphincter muscle (sphincterotomy)
Procedure: Pancreatic and Biliary Sphincterotomy
cutting the sphincter muscle (sphincterotomy)
Placebo Comparator: 2
Sham procedure; during the ERCP no sphincterotomy procedure will be performed
Procedure: ERCP
ERCP Procedure: For the procedure, you will lie on your left side on an examining table in an x-ray room. You will be given medication to help numb the back of your throat and a sedative or anesthetic to help you relax during the exam. The physician will guide the scope through your esophagus, stomach, and duodenum until it reaches the spot where the ducts of the biliary tree and pancreas open into the duodenum. The physician will the pass a small plastic tube through the scope. Through the tube, the physician will inject a dye into the ducts to make them show up clearly on x rays. X rays are taken as soon as the dye is injected


Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Patients diagnosed with the clinical syndrome of SOD, as defined by the Modified Functional Biliary Disorders Module of the Rome III criteria
  2. Pain burden of Grade 3 or higher on RAPID Questionnaire.
  3. Cholecystectomy more than 90 days before enrollment.
  4. Laboratory Tests: Results of blood tests taken within 1 week preceding the baseline visit and any others available from the preceding 6 months (post-cholecystectomy):Direct bilirubin, alkaline phosphatase, amylase and lipase results must be no greater than 2 X the upper level of normal.Transaminase levels can be no more than 3 X upper limit of normal. If the transaminases are elevated (<2X ULN) in association with a pain attack, they cannot have returned to normal within 3 days.
  5. Normal abdominal imaging by CT or MR/MRCP with bile duct reported at ≤9mm.
  6. Upper endoscopy examination without findings to explain the pain.
  7. Pain persisting despite a one trial of acid suppressant medications for one month (if tolerated).
  8. Pain persisting despite a trial of antispasmodics.
  9. Subjects on antidepressants for pain control (not required) should be taking them for a minimum of one month prior to the baseline assessment.

9.Patients with SOD with depressive and/or anxiety disorders who receive psychopharmacologic treatment must be on stable medication dose for at least 6 weeks.

10.Access to a telephone. 11.Must be able to speak, read, and write English. 12.Signed and dated informed consent.

Exclusion Criteria:

  1. Prior ERCP treatment.
  2. Age < 18 or Age > 65.
  3. Pregnancy: Women who are pregnant at the time of Screening* will be excluded from the study. (*Note: Women who become pregnant AFTER the Baseline Visit/ERCP will be allowed to remain in the study for telephone follow-up visits).
  4. Prior gastric resection or surgery involving biliary diversion.
  5. Prior diagnosis of acute pancreatitis (lipase >3 x ULN) including post-ERCP pancreatitis, or of chronic pancreatitis by radiological imaging, EUS 5 or more criteria, or Cambridge criteria moderate or more on ERCP.
  6. Daily use of prescription analgesics over the previous month.
  7. Abdominal discomfort every day for the past month at level of 3 or more on a scale of 1-10.
  8. Presence of significant psychiatric disorders:

    1. Lifetime psychotic disorders, bipolar disorder;
    2. Substance use disorders within 6 months;
    3. Eating disorders within 2 years
    4. Moderate & severe depression defined by BDI-II (Beck Depression Inventory) cutoff scores >22 (unless receiving stable psychiatric therapy for six weeks); and/or,
    5. Suicidal risk (equal to or greater than "low") using MINI suicide section or a score of greater than 0 on question 9 of the BDI.
  9. The total number of days in the previous 3 months that the subject has taken prescription analgesics due to episodes of abdominal pain is greater than the total number of days the subject had episodes of abdominal pain.
  10. Any condition that, in the investigator's opinion, makes the subject unsuitable for study participation.

ERCP Criteria:

  1. Pancreas divisum (complete or partial) (known or discovered at study ERCP).
  2. Any pathology found at ERCP (except sphincter hypertension).
  3. Failed pancreatic manometry.
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Please refer to this study by its ClinicalTrials.gov identifier: NCT00688662

United States, Connecticut
Yale University
New Haven, Connecticut, United States, 06510
United States, Indiana
Indiana University
Indianapolis, Indiana, United States, 46202
United States, Minnesota
University of Minnesota
Minneapolis, Minnesota, United States, 55415
United States, Missouri
Midwest Therapeutic Endoscopy Consultants
St Louis, Missouri, United States, 63141
United States, South Carolina
Medical University of South Carolina Digestive Disease Center
Charleston, South Carolina, United States, 29425
United States, Texas
Methodist Dallas Medical Center
Dallas, Texas, United States, 75203
United States, Washington
Virginia Mason Medical Center
Seattle, Washington, United States, 98101
Sponsors and Collaborators
Principal Investigator: Joseph Romagnuolo, MD Medical Universtiy of South Carolina
Principal Investigator: Martin Freeman, MD University of Minnesota - Clinical and Translational Science Institute
Principal Investigator: Richard Kozarek, MD Virginia Mason Medical Center
Principal Investigator: Evan Fogel, MD Indiana University
Study Chair: Peter Cotton, MD MUSC Digestive Disease Center
Principal Investigator: Paul Tarnasky, MD Digestive Health Associates of Texas
Principal Investigator: Giuseppe Aliperti, MD Midwest Therapeutic Endoscopy Consultants
Principal Investigator: Priya Jamidar, MD Yale University
  More Information

No publications provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Peter Cotton, Study Chair, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ClinicalTrials.gov Identifier: NCT00688662     History of Changes
Other Study ID Numbers: DK074739
Study First Received: May 30, 2008
Last Updated: August 31, 2012
Health Authority: United States: Federal Government

Keywords provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK):
Sphincter of Oddi Dysfunction

Additional relevant MeSH terms:
Sphincter of Oddi Dysfunction
Bile Duct Diseases
Biliary Dyskinesia
Biliary Tract Diseases
Common Bile Duct Diseases
Digestive System Diseases

ClinicalTrials.gov processed this record on October 20, 2014