Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
It is considered that the subject suffers a confirmed diagnosis of colon cancer and is going to undergo surgery on a scheduled basis under a RHMM program.
The subject is ≥ 18 years of age.
The subject can perform any of the two proposed treatments.
Preoperative staging TxNxM0.
The patient has voluntarily signed and dated an informed consent document (IC), approved by an independent Ethics Committee (CEIC) before participating in the study.
You may not be if
Patients with rectal cancer.
The subject can not give informed consent to participate in the study.
The subject can not perform the pre-habilitation.
Non-acceptance or impossibility of following rehabilitation protocol multimodal
The subject was previously scheduled at the time of the inclusion of the nutritional supplement study, whether it is different or the same that would be scheduled at this time
Subjects who have received previous radiochemotherapy, HIV, gestational stage, psychiatric, with CRF who are undergoing renal replacement techniques, urgent surgery, with intestinal obstructions, with uncontrolled infections, urgent surgery, distant metastasis, ASA IV, advanced liver failure, severe coagulation disorder, severe hyperlipidemia and hyperglycemia or difficult to control.
Subject has renal or hepatic impairment (GFR \<60ml / m or AST / ALT 3 x upper limit of normal).
Clareo Health | Effect of Prehabilitation on the Lean Mass Index (IMM) in ERAS PROGRAMM.
