Actively Recruiting
Results of the Surgical Treatment of Patients From Hepatobiliopancreatic Surgical Unit at the Complejo Hospitalario de Navarra
Led by Fundacion Miguel Servet · Updated on 2020-09-21
1000
Participants Needed
1
Research Sites
261 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the outcomes of patients who have undergone surgery by the Hepatobiliopancreatic (HPB) Surgical Unit. The study aims to assess post-surgical morbidity and mortality based on international classifications, as well as survival and disease-free survival rates for patients treated surgically for tumoral causes. This observational study includes both retrospective and prospective data collection over a long-term period. The surgical treatments involve various techniques tailored to each patient’s specific condition, performed by the HPB Surgical Unit. The study includes patients operated on in the last 10 years and those undergoing surgery from January 2019 onward who consent to participate. There are no experimental drugs; instead, the focus is on observing outcomes following these surgical procedures. Participants’ health status is monitored for 90 days after surgery to assess morbidity and mortality, while survival and disease-free survival are tracked for up to 5 years. Researchers also evaluate the standardization of pre- and post-surgical care, the effectiveness of multimodal treatments, oncological quality standards, and minimally invasive surgical techniques. The study spans several years, allowing detailed follow-up and analysis of long-term surgical results.
CONDITIONS
Brief Title
Results of Surgical Treatment of the Hepatobiliopancreatic Surgical Unit
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients operated by the HPB Surgical Unit in the last 10 years
- All patients being operated by the HPB Surgical Unit from January 2019 onwards who provide informed consent
You will not qualify if you...
- Patients not eligible for surgery
- Patients not interested in taking part in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 90 days
Participants undergo hepatobiliopancreatic surgery with different surgical techniques tailored to each patient’s pathology, followed by immediate post-operative care.
Approximately 6 post-operative visits
Duration - Up to 5 years
Participants are monitored for survival and disease-free survival rates, as well as oncological outcomes, for up to 5 years after surgery.
Visits scheduled periodically during follow-up
Trial Site Locations
Total: 1 location
1
Complejo Hospitalario de Navarra
Pamplona, Navarre, Spain, 31008
Actively Recruiting
Research Team
F
Francisco Javier Herrera Cabezón, MD
P
Pablo Sánchez Acedo, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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