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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01382680 |
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Date of registration:
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22/06/2011 |
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Primary sponsor: |
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Public title:
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Comparison of the Guide-wire G-240 to a Combination of a Flexible/Hydrophil and a Nitinol Guide Wire
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Scientific title:
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Comparison of the Use of the Guide-wire G-240 to a Combination of a Flexible/Hydrophil Guide Wire With a Nitinol Wire in Patients With Stenosis of the Bile Ducts in ERCP |
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Date of first enrolment:
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October 2010 |
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Target sample size:
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100 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01382680 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic
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Countries of recruitment
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Germany
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Contacts
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Name:
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Jörg G Albert, MD |
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Address:
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Telephone:
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+49-69-6301-5297 |
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Email:
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J.Albert@med.uni-frankfurt.de |
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Affiliation:
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Name:
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Jörg G Albert, MD |
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Address:
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Telephone:
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+49-69-6301-5297 |
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Email:
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J.Albert@med.uni-frankfurt.de |
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Affiliation:
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Name:
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Jörg G Albert, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Johann Wolfgang Goethe University Hospital and Clinics Department of Internal Medicine I |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Obstruction of the biliary tract (cross sectional imaging or ultrasonography/lab
data)
Exclusion Criteria:
- Operatively alternated anatomy of the patient.
- Intervention of the pancreatic duct.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Other Specified Diseases of Biliary Tract
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Intervention(s)
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Device: Guidewire
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Primary Outcome(s)
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Number of guidewires per ERCP session
[Time Frame: Within the same ERCP session (day 1)]
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Secondary Outcome(s)
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Time of ERCP session
[Time Frame: day 1]
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Treatment aim
[Time Frame: day 1]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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