Genetic Linkage Study for Hereditary Pancreatitis

The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2006 by Office of Rare Diseases (ORD).
Recruitment status was  Recruiting
Sponsor:
Collaborator:
University of Pittsburgh
Information provided by:
Office of Rare Diseases (ORD)
ClinicalTrials.gov Identifier:
NCT00004475
First received: October 18, 1999
Last updated: September 5, 2006
Last verified: September 2006

October 18, 1999
September 5, 2006
December 1998
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Complete list of historical versions of study NCT00004475 on ClinicalTrials.gov Archive Site
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Genetic Linkage Study for Hereditary Pancreatitis
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OBJECTIVES:

I. Establish linkage in families with hereditary pancreatitis between the phenotype and a chromosomal locus (loci) that contains the responsible gene.

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.

Observational
Observational Model: Natural History
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Pancreatitis
Procedure: genetic testing
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
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  • Diagnosis of hereditary pancreatitis with confirmation of phenotype by: Onset of pain before age 20 Amylase elevation at least 2 times normal Surgical or postmortem confirmation of pancreatitis Unequivocal evidence of pancreatic exocrine insufficiency in the absence of trauma, alcohol abuse, elevated serum lipids, or other known causes
  • Family member of a patient diagnosed with hereditary pancreatitis
Both
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United States
 
NCT00004475
199/14042, UPMC-951061, UPMC-R01DK54709-01, UPMC-R03DK51954
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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
University of Pittsburgh
Study Chair: David C. Whitcomb University of Pittsburgh
Office of Rare Diseases (ORD)
September 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP