Duloxetine in Patients With Suspected Functional Pancreatic/Biliary Pain (Sphincter of Oddi Dysfunction)

Completed · Phase 3

Conditions studied: Sphincter of Oddi Dysfunction

In brief

Open-label single center study of duloxetine in patients with SOD who have failed to respond to the standard treatments. This protocol is designed to explore the tolerability and efficacy of Duloxetine in the management of patients with known or suspected Sphincter of Oddi dysfunction (SOD).

Key facts

Study ID

NCT00471315

Run by

Medical University of South Carolina

People needed

18

Starts

2006-07-01

Expected to finish

2012-03-01

Last updated by the study team

2014-02-06

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients referred to MUSC pancreatico-biliary service for investigation/ mgt of functional upper abdominal pain symptoms;
• No clinically significant medical condition(s) as determined by the investigator;
• Symptom severity. At least 2 pain attacks in the previous month, with severity of at least 4/10 on the RAPID Start scale;
• Prior cholecystectomy;
• Age 18-65*;
• Functional pain characteristics as defined by Rome III Criteria;
• Structural causes of pain excluded by standard imaging and laboratory investigations;
• No clinically significant ECG results as determined by the investigator;
• All patients will give verbal and written Informed consent;
• Female patients must use an acceptable form of contraception, or be 2 years postmenopausal or surgically sterile*; and
• Geographically accessible for follow-up visits

You may not qualify if…

• History of/current psychosis, bipolar disorder, suicidal ideation or judged to be a significant suicide risk, as determined via baseline psychiatric assessment utilizing the MINI interview
• History of alcohol or any psychoactive substance abuse or dependence within the past 6 months, as determined via baseline psychiatric assessment utilizing the MINI interview
• Abnormal Liver Function Tests (> 3 x ULN)
• Known hypersensitivity to Duloxetine or any of the inactive ingredients
• Treatment with a monoamine oxidase inhibitor (MAOI) within 14 days of randomization or potential need to use an MAOI during study or within 5 days of discontinuation of study drug
• Treatment with fluoxetine (deleted MAOI) within 30 days of medication start date
• Treatment with excluded medications within 7 days prior to study medication start-up date
• Serious medical illness, including any cardiovascular, hepatic, renal respiratory hematologic, endocrinologic or neurologic disease, or significant laboratory abnormality as judged by study physician/investigator.
• Uncontrolled narrow-angle glaucoma
• Acute liver injury (such as hepatitis) or severe cirrhosis
• Prior lack of tolerability to duloxetine
• Pregnancy and breastfeeding
• Participation in the study is approximately 4 months. There are 4 clinic visits and 2 telephone visits.

Where it is running

• Digestive Disease Center, Medical University of South Carolina — Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

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