Actively Recruiting

Age: 18Years +
All Genders
NCT07173257

PROMs After Pancreatectomy

Led by University of Arizona · Updated on 2025-09-15

250

Participants Needed

2

Research Sites

191 weeks

Total Duration

On this page

Sponsors

U

University of Arizona

Lead Sponsor

M

Mayo Clinic - Scottsdale/Phoenix, Arizona

Collaborating Sponsor

AI-Summary

What this Trial Is About

The standard of care for a patient with resectable pancreatic is to perform pancreatic resection which, even in the modern era is associated with significant complications and impact on quality of life, often in the setting of poor survival even in the best scenario. Currently, there is a lack of data on patient quality of life after such procedures, how quality of life changes throughout the course of care, and whether patients who undergo these procedures are satisfied with their decision. This research is aimed to understand the impact of pancreatic surgery on patients' quality of life, how that impact changes over time, and patient satisfaction (or regret) with their decisions. This work will help improve the pre-operative conversation to help patients decide whether undergoing a pancreatic resection aligns with their post-operative goals of care.

CONDITIONS

Official Title

PROMs After Pancreatectomy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over 18 years old who undergo pancreatic resection for any reason
  • Patients of any race, gender, or ethnicity
  • Patients who are fluent in English
Not Eligible

You will not qualify if you...

  • Patients under 18 years old
  • Patients who are unable to provide informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Mayo Clinic - Phoenix

Phoenix, Arizona, United States, 85054

Actively Recruiting

2

The University of Arizona

Tucson, Arizona, United States, 85724

Actively Recruiting

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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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