Pediatric Liver Database
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Purpose
The purpose of this study is to collect data to examine and characterize the clinical outcomes of pediatric patients diagnosed with any liver disease at Children's Hospital of Wisconsin.
| Condition |
|---|
|
Liver Disease Liver Transplant |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Pediatric Liver Disease and Liver Transplant Database |
| Estimated Enrollment: | 500 |
| Study Start Date: | June 2003 |
| Estimated Study Completion Date: | June 2018 |
| Estimated Primary Completion Date: | June 2018 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
LD###
These child subjects have some form of liver disease (including those who need a liver transplant) or have already had a liver transplant.
|
Detailed Description:
In this study, medical information which is routinely obtained on children with any liver diseases, or children who have had a liver transplant will be entered into a database. No extra tests are done for participating in this study, and no extra visits to the doctor are required. The clinical data collected is then entered into a database and followed longitudinally. The information obtained from this study will help researchers learn more about pediatric liver disease, therefore providing better routine clinical treatment.
Eligibility| Ages Eligible for Study: | up to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
All child subjects will be recruited from the Hepatology Clinic at Children's Hospital of Wisconsin
Inclusion Criteria:
- Under 18 years of age
- newly diagnosed with a liver disease, currently listed for liver transplant, or who are being considered for liver transplantation and evaluated
- receive a liver transplant prior to their eighteenth birthday
Exclusion Criteria:
- Patients decline participation.
- Patients have no liver diseases.
Contacts and Locations| Contact: Grzegorz Telega, MD | 414-266-3690 | gtelega@mcw.edu |
| Contact: Vincent F Biank, MD | 414-266-3690 | vbiank@mcw.edu |
| United States, Wisconsin | |
| Children's Hospital of Wisconsin | Recruiting |
| Milwaukee, Wisconsin, United States, 53226 | |
| Contact: Grzegorz Telega, MD 414-266-3690 gtelega@mcw.edu | |
| Contact: Vincent F Biank, MD 414-266-3690 vbiank@mcw.edu | |
| Principal Investigator: Grzegorz Telega, MD | |
| Sub-Investigator: Vincent F Biank, MD | |
| Sub-Investigator: Jose Franco, MD | |
| Principal Investigator: | Grzegorz Telega, MD | Medical College of Wisconsin |
More Information
No publications provided
| Responsible Party: | Grzegorz Telega/Principal Investigator, Medical College of Wisconsin |
| ClinicalTrials.gov Identifier: | NCT00677625 History of Changes |
| Other Study ID Numbers: | CHW 03/64 HRRC 188-03 |
| Study First Received: | May 9, 2008 |
| Last Updated: | June 21, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Medical College of Wisconsin:
|
Liver Transplant |
Additional relevant MeSH terms:
|
Liver Diseases Digestive System Diseases |
ClinicalTrials.gov processed this record on May 23, 2013