Surgery Clinical Trial
Official title:
Longitudinal Outcomes in Hepatic Resection
NCT number | NCT02997098 |
Other study ID # | Pro00078618 |
Secondary ID | |
Status | Withdrawn |
Phase | |
First received | |
Last updated | |
Start date | May 4, 2017 |
Est. completion date | May 2037 |
Verified date | July 2018 |
Source | Duke University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
This observational registry of patients undergoing liver surgery collects patients both retrospectively and prospectively. Patients undergoing liver resection for any non-transplant indication will be evaluated for clinical outcomes (such as surgical complications, survival, and disease progression) based on clinical and patient factors (like indication, age, and other treatments for the disease).
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | May 2037 |
Est. primary completion date | May 2037 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients requiring liver resection Exclusion Criteria: - Patients under the age of 18 years - Patients undergoing liver transplant |
Country | Name | City | State |
---|---|---|---|
United States | Duke University Health System | Durham | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Duke University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Overall survival | 10 years | ||
Secondary | Disease-free survival | 10 years | ||
Secondary | Surgical-site infection | 3 months | ||
Secondary | Postoperative bleeding | 3 months | ||
Secondary | Blood clot | 3 months | ||
Secondary | Use of other therapy | e.g., antibiotics in liver abscess, chemotherapy in liver cancer | 5 years | |
Secondary | Operative time | 1 day | ||
Secondary | Intraoperative blood loss | 1 day | ||
Secondary | Number of segments resected | If applicable | 1 day |
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