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NCT00155376 Clinical Trial

Intravenous-Morphine and Glucagon-Usage Enhanced MR Cholangiography

Liver Disease Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00155376
Other study ID # 940104
Secondary ID
Status Recruiting
Phase Phase 4
First received September 8, 2005
Last updated November 25, 2005
Start date September 2005
Est. completion date September 2005

Study information
Verified date April 2005
Source National Taiwan University Hospital
Contact Yuan-Heng Mo, MD
Email jamesmyh@ha.mc.ntu.edu.tw
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Interventional

Clinical Trial Summary

Morphine can induce constriction of sphincter of oddi and glucagon can facilitate bile secretion and dilatation of bile duct. We conduct this randomized double blinded study to evaluate the effect of enhancement in MRCP using intravenous morphine and glucagon.

Description:

Morphine can induce constriction of sphincter of oddi and glucagon can facilitate bile secretion and dilatation of bile duct. We conduct this randomized double blinded study to evaluate the effect of enhancement in MRCP using intravenous morphine and glucagon.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date September 2005
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

- normal volunteer

- living liver donor

Exclusion Criteria:

- COPD

- chronic liver disease

- hypersensitive to glucagon

- DM

- insulinoma

- glucagonoma

- pregnancy

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Intervention

Drug:
• morphine and glucagon

Locations
Country Name City State
Taiwan National Taiwan University Hospital Taipei province of Taiwan

Sponsors (1)
Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary MRCP visibility
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