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New treatment option for Parenteral Nutrition
Official title Achieving nuTritional Target in criticAlly Ill patieNts With iMpairEd gastroiNtesTinal Dysfunction
ClinicalTrials.gov ID: NCT06510348
What this study is testing
- What it's testing
- Clear study hypothesis / research question It has already been proven that a prolonged negative energy balance during intensive care stay is an independent risk factor for mortality. Although it was thought that achivieng optimal delivery of calories will prevent nutritional deficits in critically ill patients, published randomized controlled trials failed to confirm this hypothesis.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- All adults (\> 18 years old)
- Mechanical ventilation for more than four days,
- Controlled shock state (hemodynamic and tissue perfusion goals are reached) - Impaired intestinal absorbtion, defiend by both ultrasound measurement...
You likely can't join if
- patients on non-invasive mechanichal ventilation
- contraindication for EN for \> 48 h after admission
- patients with gastrointestinal surgical intervention within 3 months,
- history of malabsorption, inflammatory bowel disease
- short bowel syndrom
- anorexia nervosa
See the full eligibility criteria
- All adults (\> 18 years old)
- Mechanical ventilation for more than four days,
- Controlled shock state (hemodynamic and tissue perfusion goals are reached) - Impaired intestinal absorbtion, defiend by both ultrasound measurement of gastric residual volume and paracetamol absorbtion test
- patients on non-invasive mechanichal ventilation
- contraindication for EN for \> 48 h after admission
- patients with gastrointestinal surgical intervention within 3 months,
- history of malabsorption, inflammatory bowel disease
- short bowel syndrom
- anorexia nervosa
- gastrointestinal bleeding
- cirrhosis
- traumatic brain injury
- subarahnoidal hemorrhage
- neoplasia
- post cardiac arrest patients
- patients on chronic therapy with corticosteroids
- pregnant women.
The study team makes the final eligibility decision.
Where it's taking place
- Bucharest, Romania
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Bucharest, Romania. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.