Gastrointestinal Dysfunction in Aortic Surgery Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInstituto Nacional de Cardiologia Ignacio Chavez

About this trial

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.

Eligibility criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • No intervention

Treatment groups

No treatment groups listed

Sponsors and collaborators

Instituto Nacional de Cardiologia Ignacio Chavez

Lead sponsor

Instituto Nacional de Enfermedades Respiratorias

Collaborator

National Polytechnic Institute, Mexico

Collaborator