No Study Drug
Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
114 (estimated)
Sponsor
Instituto Nacional de Cardiologia Ignacio Chavez · Other
Who this trial is looking for
This trial is looking for patients who are 18 or older and have undergone surgery on the aorta. Participants will help researchers understand how gastrointestinal problems relate to recovery in intensive care after surgery.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years of age or older.
I have had surgery on my aorta.
I need mechanical ventilation for more than 48 hours.
I have signed the informed consent form.
You may not be able to join if
I have pre-existing gastrointestinal issues.
I have been diagnosed with adult congenital heart disease.
I am currently pregnant or breastfeeding.
I am participating in another clinical study with experimental treatment.
I have chronic intestinal disease.
I have had gastrointestinal problems in my nutritional screening.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The goal of this observational study is to determine the association of gastrointestinal dysfunction through the Gastrointestinal Dysfunction Scale (GIDS) tool and serum concentrations of citrulline and Intestinal fatty-acid binding protein (I-FABP) with primary \[calories received, protein received, parenteral nutrition requirement and 28-day mortality in the intensive care unit (ICU)\] and secon…
The goal of this observational study is to determine the association of gastrointestinal dysfunction through the Gastrointestinal Dysfunction Scale (GIDS) tool and serum concentrations of citrulline and Intestinal fatty-acid binding protein (I-FABP) with primary \[calories received, protein received, parenteral nutrition requirement and 28-day mortality in the intensive care unit (ICU)\] and secondary (development of pneumonia, surgical and cardiovascular complications in the ICU, length of hospital and ICU stay, duration of mechanical ventilation) clinical outcomes in critically ill patients undergoing aortic surgery.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 18 years of age or older.
* Patients after surgical interventions (elective or urgency) on the aorta with cardiopulmonary bypass.
* Invasive mechanical ventilation expected to be required more than 48 hours.
* Signed informed consent.
Exclusion Criteria:
* Patients under mec…
Inclusion Criteria:
* 18 years of age or older.
* Patients after surgical interventions (elective or urgency) on the aorta with cardiopulmonary bypass.
* Invasive mechanical ventilation expected to be required more than 48 hours.
* Signed informed consent.
Exclusion Criteria:
* Patients under mechanical ventilation with pre-existing gastrointestinal issues.
* Diagnosis of adult congenital heart disease.
* Ongoing pregnancy or lactation period.
* Simultaneous participation in another clinical study involving experimental therapy.
* Presence of chronic intestinal disease.
* Previous gastrointestinal conditions detected during nutritional screening.
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