Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04469504

Preoperative Prehabilitation for Sarcopenic Patients Prior to Pancreatic Surgery for Cancer

Led by University Hospital, Lille · Updated on 2023-02-08

158

Participants Needed

1

Research Sites

310 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Lille

Lead Sponsor

G

Groupement Interrégional de Recherche Clinique et d'Innovation

Collaborating Sponsor

AI-Summary

What this Trial Is About

Major digestive surgery is associated with a significant rate of postoperative complications. To improve postoperative outcome, efforts are focused on postoperative course leading to the concept of rehabilitation. However, the rehabilitation concept does not allow to improve muscular and functional reserves at the time of surgery. Sarcopenia is a condition characterized by loss of skeletal muscle mass and function. Also, the prevalence of sarcopenia in patients with cancer is high and has a prevalence of around 25% in patients with pancreatic cancer, with a considerable impact on postoperative and survival outcomes. The hypothesis is the preoperative management of sarcopenia by a rehabilitation program could improve patients' operative outcomes by reducing the rate of postoperative complications.

CONDITIONS

Official Title

Preoperative Prehabilitation for Sarcopenic Patients Prior to Pancreatic Surgery for Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing pancreaticoduodenectomy for cancer
  • Sarcopenic status
Not Eligible

You will not qualify if you...

  • Age younger than 18 years
  • Medical contraindications including cardiovascular disease or clinically significant vascular disease
  • Physical inability to exercise
  • Emergent surgery

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hop Claude Huriez Chu Lille

Lille, France

Actively Recruiting

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Research Team

M

Mehdi ELAMRANI, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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