search
Back to results

A Study of Serial Magnetic Resonance Cholangiopancreatography (MRCP) Following Morphine-neostigmine and Secretin Provocation in Healthy Volunteers

Primary Purpose

Sphincter of Oddi Dysfunction

Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Morphine
Neostigmine
0.9% saline
Secretin
0.9% saline
Sponsored by
University of Nottingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Sphincter of Oddi Dysfunction focused on measuring Bile ducts, Sphincter of Oddi, Pancreatic ducts

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy age matched and sex matched volunteers
  • No history of chronic abdominal pain
  • No previous abdominal surgery
  • No history suggestive of gastrointestinal motility disorders
  • No history of regular medication or substance abuse

Exclusion Criteria:

  • Acute illness within preceding 6 weeks
  • Participation in another study within 3 months
  • Allergy to morphine or neostigmine
  • Pregnancy
  • Refusal to consent to the study

Sites / Locations

  • University of Nottingham

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Morphine-neostigmine

Secretin

Arm Description

Outcomes

Primary Outcome Measures

Serum amylase (U/L)
Serum lipase (U/L)
Liver function tests

Secondary Outcome Measures

Pancreatic duct diameter (mm)
Pancreatic duct length (mm)
Common bile duct diameter (mm)
Gallbladder volume (mm3)

Full Information

First Posted
May 28, 2010
Last Updated
June 1, 2010
Sponsor
University of Nottingham
search

1. Study Identification

Unique Protocol Identification Number
NCT01134848
Brief Title
A Study of Serial Magnetic Resonance Cholangiopancreatography (MRCP) Following Morphine-neostigmine and Secretin Provocation in Healthy Volunteers
Official Title
A Randomised, Double Blind Cross-over Study of Serial MRCP Following Morphine-neostigmine and Secretin Provocation in Healthy Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
May 2010
Overall Recruitment Status
Completed
Study Start Date
January 2009 (undefined)
Primary Completion Date
February 2010 (Actual)
Study Completion Date
February 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Nottingham

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The sphincter of Oddi is a circular band of muscle which controls the flow of pancreatic juices and bile into the small intestine. Abnormal function of the Sphincter of Oddi, known as Sphincter of Oddi dysfunction (SOD), can lead to recurrent episodes of abdominal pain. Making a diagnosis of SOD is difficult and is currently achieved using an invasive pressure test. This pressure test is associated with some adverse effects including inflammation of the pancreas gland. We are investigating an alternative test in which medication is given to provoke spasm of the sphincter. Following provocation, blood can be sampled to detect changes in blood composition and changes in sphincter anatomy can be evaluated using specialized imaging techniques. Our aim is to study and compare the effects of two provocation medications (morphine-prostigmine and secretin) on biliary and pancreatic ductal anatomy, using dynamic serial MRCP in healthy volunteers. Our hypothesis is that morphine-neostigmine provocation results in greater changes in biliary and pancreatic ductal anatomy when assessed using dynamic serial MRCP.
Detailed Description
The sphincter of Oddi (SO), which encases the distal common bile duct (CBD) and pancreatic duct (PD), comprises a fibromuscular complex to control the flow of biliary and pancreatic secretions into the duodenum. Aberrant function of the SO, known as Sphincter of Oddi dysfunction (SOD), can lead to recurrent episodes of biliary or pancreatic type pain. Both surgical sphincteroplasty and endoscopic sphincterotomy can improve symptoms in some patients who are suspected to have SOD. However, poor results are obtained in a significant proportion reflecting the difficulties in achieving an accurate diagnosis and also in selecting those patients likely to benefit from these procedures. A number of investigative modalities have been employed in the assessment of SOD. Of the available diagnostic tests sphincter of Oddi manometry (SOM) is considered the gold standard, but is associated with a high rate of post procedure morbidity including pancreatitis and biliary sepsis. It is therefore unsurprising that attention has focussed on non-invasive diagnostic tests. Developments in magnetic resonance cholangiopancreatography (MRCP) have allowed for the detailed non-invasive assessment of biliary and pancreatic ductal morphology and can be used in conjunction with intravenous secretin provocation (ss-MRCP). Evaluations of this technique have so far been disappointing, demonstrating only a modest concordance with SOM in patients suspected with SOD. The morphine-prostigmine provocation test (Nardi test) has previously been utilised as a screening test in patients with symptoms suggestive of SOD. It is performed by giving an intramuscular injection of morphine 10mg and prostigmine 1mg, with a positive test indicated by the reproduction of pain or a fourfold increase in either serum amylase or lipase levels. As enzymatic changes have been shown to occur in healthy subjects and in those with irritable bowel syndrome, the test has largely fallen out of favour. However, a recent publication has suggested morphine used as a pharmacological provocation agent can improve ductal distension and aid the differentiation of pancreaticobiliary variants on MRCP. To date this has not been investigated in a randomised or blinded study and we have therefore proposed to examine the effects of morphine-neostigmine and secretin provocation on gallbladder volume and biliary and pancreatic ductal morphology in healthy volunteers using serial MRCP.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sphincter of Oddi Dysfunction
Keywords
Bile ducts, Sphincter of Oddi, Pancreatic ducts

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Morphine-neostigmine
Arm Type
Active Comparator
Arm Title
Secretin
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Morphine
Intervention Description
10mg IM
Intervention Type
Drug
Intervention Name(s)
Neostigmine
Intervention Description
1mg IM
Intervention Type
Drug
Intervention Name(s)
0.9% saline
Intervention Description
0.1 ml/kg
Intervention Type
Drug
Intervention Name(s)
Secretin
Intervention Description
1 unit/kg IV
Intervention Type
Drug
Intervention Name(s)
0.9% saline
Intervention Description
1ml IM
Primary Outcome Measure Information:
Title
Serum amylase (U/L)
Time Frame
0, 60, 120, 180 and 240 minutes
Title
Serum lipase (U/L)
Time Frame
0, 60, 120, 180 and 240 minutes
Title
Liver function tests
Time Frame
0, 60, 120, 180 and 240 minutes
Secondary Outcome Measure Information:
Title
Pancreatic duct diameter (mm)
Time Frame
0, 5, 30, 60, 90, 120, 150 and 180 minutes
Title
Pancreatic duct length (mm)
Time Frame
0, 5, 30, 60, 90, 120, 150 and 180 minutes
Title
Common bile duct diameter (mm)
Time Frame
0, 5, 30, 60, 90, 120, 150 and 180 minutes
Title
Gallbladder volume (mm3)
Time Frame
0, 5, 30, 60, 90, 120, 150 and 180 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy age matched and sex matched volunteers No history of chronic abdominal pain No previous abdominal surgery No history suggestive of gastrointestinal motility disorders No history of regular medication or substance abuse Exclusion Criteria: Acute illness within preceding 6 weeks Participation in another study within 3 months Allergy to morphine or neostigmine Pregnancy Refusal to consent to the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dileep Lobo, MBBS DM FRCS
Organizational Affiliation
University of Nottingham
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Abeed Chowdhury, MB ChB BSc MRCS
Organizational Affiliation
University of Nottingham
Official's Role
Study Director
Facility Information:
Facility Name
University of Nottingham
City
Nottingham
State/Province
Nottinghamshire
ZIP/Postal Code
NG7 2UH
Country
United Kingdom

12. IPD Sharing Statement

Learn more about this trial

A Study of Serial Magnetic Resonance Cholangiopancreatography (MRCP) Following Morphine-neostigmine and Secretin Provocation in Healthy Volunteers

We'll reach out to this number within 24 hrs