Cholangiocarcinoma Clinical Trial
Official title:
Long-term Morbidity After Surgery for Perihilar Cholangiocarcinoma; a Cohort Study
NCT number | NCT03999593 |
Other study ID # | 0001 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | January 2009 |
Est. completion date | October 2017 |
Verified date | June 2019 |
Source | University of Liverpool |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Surgery for perihilar cholangiocarcinoma offers the only possibility of long-term survival,
but remains a formidable undertaking. Traditionally, 90 day post-operative complications and
death have been used to define operative risk. However, there is concern that this metric may
not accurately capture long-term morbidity after such complex surgery.
This is a retrospective review of a prospective database of patients undergoing surgery for
perihilar cholangiocarcinoma at a Western centre between 2009-2017.
Status | Completed |
Enrollment | 60 |
Est. completion date | October 2017 |
Est. primary completion date | October 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: •Macroscopically complete resection of Bismuth 2-4 (peri)hilar cholangiocarcinoma with curative intent Exclusion Criteria: - Metastatic disease - Failure of curative intent resection (as per operating surgeon) - Post resection histopathological diagnosis other than cholangiocarcinoma |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Liverpool |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Perioperative morbidity | Clavien-Dindo complication index | 30 day | |
Secondary | Perioperative morbidity | Clavien-Dindo complication index | 90 day |
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