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Prognosis and Diagnosis of Acute Gastrointestinal Dysfunction in Cardiac Surgery Patients

Prognosis and Diagnosis of Acute Gastrointestinal Dysfunction in Cardiac Surgery Patients

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07422246
Acronym
PREDICT-GICS
Enrollment
100
Registered
2026-02-19
Start date
2026-03-10
Completion date
2028-09-30
Last updated
2026-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Surgery, Cardiac Surgery in Adult Patient, Cardiac Surgery Intensive Care Treatment, Gastrointestinal Dysfunction

Keywords

cardiac surgery, intestinal dysfunction, gastrointestinal dysfunction, gastrointestinal complications, multiorgan dysfunction syndrome, intestinal failure, gastrointestinal failure

Brief summary

The purpose of this prospective observational clinical cohort study is to develop a scientifically based approach to the prediction and early diagnosis of intestinal dysfunction in cardiac surgery patients. The main questions that the study should answer: What are the main risk factors for the development of intestinal dysfunction? What specific and non-specific biomarkers can predict the development of intestinal dysfunction? The study participants will be monitored from the moment of hospitalization until the end of their stay in a medical facility

Detailed description

Despite the low incidence rate from 1% to 2.5%, acute intestinal dysfunction is the cause or key link in the development and progression of multiorgan dysfunction and sepsis, which, in turn, contributes to an increase in the length of hospital stay, the need for additional diagnostic and/or therapeutic interventions, including surgical, and is also associated with high mortality (Mishra et al. 2021, Shvartsova et al. 2024). Acute intestinal dysfunction is understood as combined disorders of the motor, secretory, digesting, absorption and barrier functions of the intestine, leading to the upward contamination of conditionally pathogenic microbiota from the distal to the proximal sections, the development of uncontrolled translocation of microbes and their metabolites into the blood, which leads to the shutdown of the small intestine from the interstitial metabolism, creates the prerequisites for irreversible disorders of the main indicators homeostasis (Machulina I.A., Shestopalov A.E., Evdokimov E.A. 2020, Popova T.S., Tamazashvili T.S., Shestopalova A.E. 1991). A feature of acute intestinal dysfunction is an extremely nonspecific clinical and laboratory findings and the absence of widely available organ-specific markers. These reasons do not allow the development of complications to be detected early enough. Currently, most of the literature data is devoted mainly to the statistical description of the incidence, type of abdominal complications and outcome in patients with cardiac surgery. Acute intestinal dysfunction is not included in the list of organ systems tested to determine the severity of organ dysfunctions. SOFA due to the lack of a reliable diagnostic tool. Measurement data of intra-abdominal pressure, peristalsis activity, and volume of gastric contents in gastrostasis are most often used to monitor intestinal dysfunction. .The present study aims to explore the possibilities of verification of intestinal dysfunction by combining test results on specific and non-specific scales and dynamics of the level of molecular biomarkers; and to offer a tool for forecasting and early diagnosis

Interventions

DIAGNOSTIC_TESTadditional blood testing for specific and non-specific markers of intestinal dysfunction, ultrasound examination of abdominal organs and measurement of intra-abdominal pressure

additional blood testing for specific and non-specific markers of intestinal dysfunction, ultrasound examination of abdominal organs and measurement of intra-abdominal pressure

Sponsors

Petrovsky National Research Centre of Surgery
Lead SponsorOTHER
Negovsky Reanimatology Research Institute
CollaboratorOTHER_GOV
Lomonosov Moscow State University Medical Research and Educational Center
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* Surgery on the heart and main vessels with a high risk of developing gastrointestinal dysfunction (according to literature data and our own retrospective study); * Patient's consent to participate in the study

Exclusion criteria

* Patient's refusal to participate in the study; * HIV infection in the patient; * Immunosuppressive therapy; * Oncological disease;

Design outcomes

Primary

MeasureTime frameDescription
Identification of markers of intestinal dysfunction:During the first 24h after surgery for all patients. On the third, sixth and ninth day, if the patient stay in the ICUIntra-abdominal hypertension of 2 or more degrees and/or gastrostasis (stomach volume \>1.5ml / kg body weight measured no earlier than 4 hours after the last meal); Abdominal compartment syndrome
The use of pharmacological stimulation of gastrointestinal motilityDuring the first 24h after surgery for all patients. On the third, sixth and ninth day, if the patient stay in the ICU

Secondary

MeasureTime frame
Hospital mortalityDuring the first 24h after surgery for all patients. On the third, sixth and ninth day, if the patient stay in the ICU
Number of days spent in the ICUDuring the first 24h after surgery for all patients. On the third, sixth and ninth day, if the patient stay in the ICU
Total duration of vasopressor supportDuring the first 24h after surgery for all patients. On the third, sixth and ninth day, if the patient stay in the ICU
The dynamics of the severity of the course on the scale of sequential organ dysfunction (SOFA/SOFA-2) in patients with intestinal dysfunction in the framework of multiorgan dysfunction;During the first 24h after surgery for all patients. On the third, sixth and ninth day, if the patient stay in the ICU
Total duration of mechanical lung ventilationDuring the first 24h after surgery for all patients. On the third, sixth and ninth day, if the patient stay in the ICU
Surgical interventions on abdominal organsDuring the first 24h after surgery for all patients. On the third, sixth and ninth day, if the patient stay in the ICU

Countries

Russia

Contacts

CONTACTMaxim A. Babaev
maxbabaev@mail.ru+7-916-026-9066
CONTACTPetr V. Ageev
ageev.petia@yandex.ru+7-985-827-0461

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026