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Prognosis and Diagnosis of Acute Gastrointestinal Dysfunction in Cardiac Surgery Patients

NCT07422246 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2026-02-19

No results posted yet for this study

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

Conditions

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

Interventions

DIAGNOSTIC_TEST

additional 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 & Collaborators

  • Negovsky Reanimatology Research Institute

    collaborator OTHER_GOV

  • Lomonosov Moscow State University Medical Research and Educational Center

    collaborator OTHER

  • Petrovsky National Research Centre of Surgery

    lead OTHER

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
95 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-10
Primary Completion
2028-09-01
Completion
2028-09-30

Countries

  • Russia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07422246 on ClinicalTrials.gov