Fondazione Policlinico Universitario Agostino Gemelli, IRCCS
Rome, Italy
Location status: Recruiting
NCT Number: NCT05938322
Patients with locally advanced non-metastatic adenocarcinoma of the rectum undergoing chemoradiation therapy will be assigned to 2 groups:
* the intervention group will be prescribed an individualized ketogenic eating plan to be followed throughout the treatment period * the control group will be prescribed a diet therapy plan treatment following the international guidelines of clinical nutrition, also to be followed during treatment
Interested in participating?
Request Info18 year–75 year
All sexes
Interventional
Not applicable
Rome, Italy
Location status: Recruiting
Some days before the start of radiotherapy there will be the first visit in which patients will be enrolled and placed in one of the following two groups:
Compliance with diet therapy treatment (SD vs. KD) will be assessed by analysis of a food diary that the patient will be asked to complete.
During follow-ups it will be assessed:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
In the group of intervention is prescribed a ketogenic diet plan characterized by the following composition: carbohydrates < 30g/day, 1.2g-1.5g protein/kg/day and lipids > 65%.
This diet will be followed during the period of treatment with chemo-radiotherapy (5 weeks)
The control group (SD) will follow the Mediterranean diet pattern based on ESPEN guidelines (carbohydrates 45-55%, protein 15-20% and lipids 30-35%).
Time frame: 2 months
The primary objective is to assess the adherence to the diet therapy treatment plan (SD vs. KD). It will be verified through a food diary that will be given to the patient during the first visit.
The patients will fill out the questionnaire and return it at future visits.
Time frame: 2 months
The assessment will be carried out through the use of an impedance analysis (BIA)
Time frame: 2 months
The assessment will be carried out through the use of an impedance analysis (BIA)
Time frame: 2 months
The assessment will be carried out through blood test analysis
Time frame: 2 months
The assessment will be carried out through blood test analysis
Time frame: 2 months
Radiotherapy interruptions will be evaluated
Time frame: 2 months
The assessment will be carried out through pelvic MRI analysis, clinical evaluation, and pathological response
Time frame: 2 months
Investigating patients' quality of life through questionnaires administered at the beginning and at the end of treatments. The questionnaires used are EORT ( European Organisation for Research and Treatment of Cancer) QLQ (quality of life questionnaire)-30, QLQ - CR29 and CAX-24 (cancer cachexia-specific questionnaire), and PRT-20 (quality of life questionnaire for proctitis).
Contact information is provided by the study sponsor or research team.
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Other
Compliance With Ketogenic Diet in Patients Undergoing Radiotherapy for Pelvic Cancers: a Prospective, Randomized, Mono-centric Study
Acronym: KOMPARC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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