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Early versus postponed supplementary parenteral nutrition after major emergency abdominal surgery
EU CTIS ID: 2023-505378-14-00
What this study is testing
To compare the effect of early and postponed supplementary parenteral nutrition on the risk of postoperative nosocomial infections following major emergency abdominal surgery.
- Therapeutic use (Phase IV)
A plain-language read of the study's public EU CTIS listing. The study team confirms the details.
Who can take part
You may be able to join if
- Aged 18 or above
- Primary midline laparotomy or laparoscopy in an acute or sub-acute setting
- NRS-2002 score < 7
- No contraindications for oral or enteral intake after surgery
- Intake of less than 50% of recommended caloric target on second postoperative day
- Ability to provide informed consent
You likely can't join if
- Refusal to participate in the study
- Damage control laparotomy
- Laparoscopic appendectomy or laparoscopic cholecystectomy as the sole procedure
- Remaining life expectancy < 3 months
- Pregnant or breastfeeding women
- Preoperative NRS-2002 score = 7
See the full eligibility criteria
- Aged 18 or above
- Primary midline laparotomy or laparoscopy in an acute or sub-acute setting
- NRS-2002 score < 7
- No contraindications for oral or enteral intake after surgery
- Intake of less than 50% of recommended caloric target on second postoperative day
- Ability to provide informed consent
- Refusal to participate in the study
- Damage control laparotomy
- Laparoscopic appendectomy or laparoscopic cholecystectomy as the sole procedure
- Remaining life expectancy < 3 months
- Pregnant or breastfeeding women
- Preoperative NRS-2002 score = 7
- Limiting mental or psychiatric disorders rendering participation unethical or unrealistic
- Need for parenteral nutrition before second postoperative day
The study team makes the final eligibility decision.
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
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, 18-64 years, 65+ years. The study team makes the final eligibility decision.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.