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Patient Reported Outcomes Measures to Predict Pancreatic Surgery Outcomes

NCT04431076 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 560

Last updated 2024-01-18

No results posted yet for this study

Summary

This is a prospective single-center observational study with the mail objective to identify specific subgroups of patients planned for pancreatic resection, at high risk for postoperative morbidity and impaired recovery through preoperative screening of physical, functional, nutritional and psychological risk factors using patient reported questionnaires and performance tests.

Consecutive patients planned for pancreatic resection will be enrolled to screen for physical, functional, nutritional and psychological risk factors. The study duration is 3 years: 2 years of recruitment and 1 year of follow-up.

The findings of the present study will enable researchers to identify specific risk categories to plan personalized prehabilitation programs and modulate oncologic treatment strategies in cancer patients planned for pancreatic surgery.

Conditions

  • Pancreatic Cancer
  • Patient Reported Outcome Measures
  • Quality of Life
  • Pancreatectomy
  • Nutritional Status
  • Recovery of Function

Sponsors & Collaborators

  • Massimo Falconi

    lead OTHER

Principal Investigators

  • Nicolò Pecorelli, Surgeon · Ospedale San Raffaele IRCCS

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-05-07
Primary Completion
2022-08-30
Completion
2024-06-30

Countries

  • Italy

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04431076 on ClinicalTrials.gov