Actively Recruiting

Age: 15Years - 90Years
All Genders
ID04556019

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

Age: 15Years - 90Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

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

Long-term Monitoring

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

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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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