Actively Recruiting

Phase Not Applicable
Age: 70Years +
All Genders
NCT05491434

Sarcopenia in Colorectal Cancer Patients, Intervention Study

Led by Hospital Universitari de Bellvitge · Updated on 2025-05-20

370

Participants Needed

1

Research Sites

269 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The sarcopenia is a new concept for evaluating the functional status of patients, introduced during the last 20 years. This is defined as the relationship between the deterioration of muscle mass and the decrease in strength, the metabolic rate, the aerobic capacity and subsequently the evaluation of the functional status. The sarcopenia has been estimated to affect 5% to 13% of people aged between 60 and 70 years, increasing from 11% to 50% in those aged 80 years and older. In a study by Lieffers et al. of a total of 234 patients with colorectal cancer, with a mean age of 63 years according to the values observed by Prado et al., the prevalence of sarcopenia would be around 39%, being able to reach up to 60% in patients with chronic diseases. The goal of this study is to compare the cumulative incidence of post-surgical complications due to infection at 30 days between the group of patients without sarcopenia and the group of patients with sarcopenia with an intervention based on a nutritional supplement + physical exercise.

CONDITIONS

Official Title

Sarcopenia in Colorectal Cancer Patients, Intervention Study

Who Can Participate

Age: 70Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 70 years or older
  • Diagnosed with colon adenocarcinoma without synchronous metastases
  • No urgent surgery needed
  • ECOG performance status of 2 or less
  • Not pregnant or lactating
  • Signed informed consent form
  • Able to follow study instructions
Not Eligible

You will not qualify if you...

  • Diagnosis of rectal cancer
  • Any other cancer in the last 5 years
  • Medical or mental condition preventing informed consent
  • Uncontrolled or stable medical conditions
  • Clinically significant heart disease such as congestive heart failure or symptomatic coronary disease
  • Refusal to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital Universitari de Bellvitge

L'Hospitalet de Llobregat, Barcelona, Spain, 08709

Actively Recruiting

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Research Team

R

Ricardo Frago, Ph D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

CROSSOVER

Primary Purpose

PREVENTION

Number of Arms

2

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