Impact of Various Diets on Surgical Complications
- Conditions
- Complication,Postoperative
- Registration Number
- NCT05069402
- Lead Sponsor
- Stanley Dudrick's Memorial Hospital
- Brief Summary
The optimalisation of the health status of patients scheduled for major surgery has been considered to be the most important point of perioperative care, and nutritional intervention has been perceived a key point of that intervention. Immunomodulating diets were thought to reduce cmplications, hoever recent studies put that opnion in doubt. This study was designed to assess the actual clinical significance of oral immunonutrition.
- Detailed Description
The optimalisation of the health status of patients scheduled for major surgery has been considered to be the most important point of perioperative care, and nutritional intervention has been perceived a key point of that intervention. Italian studies followed by metanalyses demonstrated the superiority of immunomodulating diets (IM) over any other preoperative nutrition, hence the surgical guidelines for enteral nutrition published by European Society for Clinical Nutrition and Metabolism (ESPEN) in 2006 recommended to use IM for 7-14 days preoperatively in all patients undergoing major surgeries. Some authors questioned IM by showing no benefit of IM over standard enteral nutrition. Other authors observed similar results.The debate was far from being over - in 2015 a new metanalysis stated that perioperative enteral nutrition is the best option for managing clinical status of patients who underwent selective surgery for gastrointestinal cancer. One year later, ESPEN changed its surgical recommendations and advised to use IM preoperatively in malnourished and perioperatively in well-nourished patients. American recommendations remained unchanged and, according to them, it is advised to use IM preoperatively in all surgical patients, however, high-protein nutrition could also be an beneficial option.
To address those doubts and to assess the actual clinical significance of oral immunonutrition, a randomized, two center, prospective clinical trial was conducted.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 300
- no sign of malnutrition (defined as one of the following unintentional weight loss by at least 10% or body mass index (BMI) < 18),
- good general status (Karnofsky Performance Index > 80,
- Eastern Cooperative Oncology Group (ECOG) grade 0 or 1);
- no confirmed neoplastic dissemination no severe concomitant disease (heart, lung, kidney, liver failure, chronic obstructive pulmonary disease [COPD], coronary aortic bypass graft [CABG], etc.),
- no history of known allergies or drug intolerance to analyzed substances.
- Patients malnourished or with metastatic disease,
- pregnant,
- in poor general status (Karnofsky <80, Eastern Cooperative Oncology Group (ECOG) > 1),
- recent history of severe heart, lung, kidney or liver failure,
- history of allergies or drug intolerance
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Infectious complications 6 months Number and type of infectious complications
Surgical complications 6 months Number and type of surgical complications
- Secondary Outcome Measures
Name Time Method Length of stay 6 months Days of hospital stay after the operation
Related Research Topics
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Trial Locations
- Locations (2)
Narodowy Instytut Onkologii
🇵🇱Krakow, Malopolska, Poland
Stanley Dudrick's Memorial Hospital
🇵🇱Skawina, Malopolska, Poland
Narodowy Instytut Onkologii🇵🇱Krakow, Malopolska, PolandStanislaw Klek, PhDContact60293566stanislaw.klek@onkologia.krakow.pl