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Impact of Perioperative Sepsis on Inflammatory, Cardiac, Coagulation, and microRNA Profiles in Patients Undergoing Major Abdominal Surgery

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

This single-center, prospective, observational study evaluates the impact of perioperative sepsis on inflammatory response, coagulation abnormalities, cardiac dysfunction, and microRNA expression in adult patients undergoing major abdominal surgery. Forty patients are enrolled and classified into septic and non-septic groups according to international sepsis definitions based on SOFA score criteria. Clinical, biochemical, echocardiographic, and molecular parameters, including selected microRNAs, are assessed preoperatively and within the first 24 hours postoperatively. The study aims to characterize pathophysiological differences associated with perioperative sepsis and to explore the potential prognostic value of microRNAs as early biomarkers of postoperative sepsis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥18 years

• Undergoing major abdominal surgery (elective or emergency)

• Ability to provide written informed consent

• Availability of biological samples in the preoperative period and within 24 hours postoperatively

• Preoperative hemodynamic stability

Locations
Other Locations
Romania
Institutul Clinic Fundeni
RECRUITING
Bucharest
Contact Information
Primary
Sebastian I Isac, Assist. Prof.
sebastian.isac@umfcd.ro
0040744543736
Backup
Buzatu Cristina
cristina.buzatu944@gmail.com
0040727391477
Time Frame
Start Date: 2026-01-20
Estimated Completion Date: 2026-04-10
Participants
Target number of participants: 40
Treatments
Septic
Patients with confirmed or suspected infection associated with an increase in SOFA score ≥2 points from baseline during the perioperative period.
Non-septic
Patients undergoing major abdominal surgery without clinical or biological evidence of sepsis.
Related Therapeutic Areas
Sponsors
Leads: Carol Davila University of Medicine and Pharmacy

This content was sourced from clinicaltrials.gov