Perioperative Sepsis. An Epigenetic Perspective

Recruiting Observational Study
Sepsis Abdominal
No Placebo Group Every participant receives an active treatment — no one gets a placebo. 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
40 (estimated)
Sponsor
Carol Davila University of Medicine and Pharmacy · Other
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About This Trial
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 criteri…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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 Exclusion Criteria…
Contacts

Sebastian I Isac, Assist. Prof.

0040744543736

sebastian.isac@umfcd.ro

CONTACT

Buzatu Cristina

0040727391477

cristina.buzatu944@gmail.com

CONTACT