Intestinal permeability 'leaky gut' in critically ill patients
- Conditions
- Critical illnessIncreased intestinal permeabilityInfection/ sepsisOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colonDiet and Nutrition - Other diet and nutrition disordersInfection - Other infectious diseases
- Registration Number
- ACTRN12616001101471
- Lead Sponsor
- a Trobe University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 40
Adult patients aged greater than or equal to 18 years;
- Patients receiving or suitable for enteral feeding;
- Likely to be admitted to the ICU for greater than or equal to 3 days;
- Likely to require mechanical ventilation for > 24 hours;
- Patients with an indwelling catheter in situ;
- Patients receiving inotropic or vasopressor support at time of enrolment.
- A past history of gut abnormalities, abdominal surgery within 2 years of ICU admission or malabsorption syndromes;
- Presenting condition or past history of abdominal trauma within 2 years of admission;
- Patients treated with therapeutic hypothermia during admission;
- Patients requiring continuous renal replacement therapy;
- Patients treated with non-steroidal anti-inflammatory drugs;
- Any situation where lactulose or any of the test sugars are used as part of the treatment plan;
- Patients receiving total parenteral nutrition or enteral feeding directly into the small bowel;
- Patients receiving or received chemotherapy or radiotherapy in the past 6 months;
- Pregnancy;
- When participation in the study is not believed to be in the best interest of the patient as determined by the treating physician.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method