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| Sponsors and Collaborators: |
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) University of Pittsburgh |
| Information provided by: | Office of Rare Diseases (ORD) |
| ClinicalTrials.gov Identifier: | NCT00004475 |
Purpose
OBJECTIVES:
I. Establish linkage in families with hereditary pancreatitis between the phenotype and a chromosomal locus (loci) that contains the responsible gene.
| Condition | Intervention |
|
Pancreatitis |
Procedure: genetic testing |
| Study Type: | Observational |
| Study Design: | Natural History |
| Study Start Date: | December 1998 |
PROTOCOL OUTLINE: This is a genetics study. Blood samples are collected from patients and family members. DNA is extracted from the blood and used for genotypic analysis and linkage analysis.
Patients do not necessarily receive the results of the genetic testing and the results do not influence the type or duration of treatment.
Eligibility
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Contacts and Locations| United States, Pennsylvania | |||||
| University of Pittsburgh, Presbyterian University Hospital | Recruiting | ||||
| Pittsburgh, Pennsylvania, United States, 15213-2582 | |||||
| Contact: David C. Whitcomb 412-648-9115 | |||||
| Contact: Beth D. Elinoff 888-748-8362 elinoffb@msx.dept-med.pitt.edu | |||||
| National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| University of Pittsburgh |
| Study Chair: | David C. Whitcomb | University of Pittsburgh |
More Information
| Study ID Numbers: | 199/14042, UPMC-951061, UPMC-R01DK54709-01, UPMC-R03DK51954 |
| First Received: | October 18, 1999 |
| Last Updated: | September 5, 2006 |
| ClinicalTrials.gov Identifier: | NCT00004475 |
| Health Authority: | United States: Federal Government |
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