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Evaluation of Glycocalyx in Major Abdominal and Thoracic Surgery

V

Vall d'Hebron University Hospital (HUVH)

Status

Unknown

Conditions

Major Elective Abdominal and Thoracic Surgery

Study type

Observational

Funder types

Other

Identifiers

NCT04900779
PR(AG)569/2020

Details and patient eligibility

About

Background:

The glycocalyx is a fundamental component of the endothelial barrier and alterations at this level have been shown to exacerbate the inflammatory response in the microcirculation. Its degradation in the surgical patient, has been tested in interventions that involve regional or general ischemia, for example in cardiac surgery, major vascular surgery or transplantation. On interventions that do not involve ischemic events the literature is limited, such is the case of those patients undergoing major abdominal and thoracic surgery.

Objective:

Assess whether there is a glycocalyx degradation in major elective abdominal and thoracic surgery, measured as an increase in plasma syndecane-1 levels during the first 24 hours of postoperative care.

Methodology:

Prospective observational study in patients undergoing major elective thoracic and abdominal surgery at the University Hospital Vall d´Hebrón. Measurement of the syndecane-1 plasma levels are going to be done during the first 24 hours after the intervention. It is intended to evaluate whether its elevation is related to anesthetic perioperative factors, and if it has an impact con morbildity and mortality in the following 6 months after the procedure.

Enrollment

117 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients older than 18 years old
  • Patients that are scheduled to major abdominal and thoracic elective surgery in Universtity Hospital Vall d´ Hebrón.
  • Patients ASA I, II and III.
  • Patients that after the intervention have their recovering in the Surgical ICU

Exclusion criteria

  • Patients ASA IV and V.
  • Patients that are hospitilized previous to the surgery.
  • Patients that undergo emergent surgery.
  • Patients with Chronic or Acute Renal Failure previous to the surgery.
  • Patients with past medical history of autoinmune disseases.
  • Patients with an active infection previous to the surgery.
  • Patients in treatment with steroids previous to the surgery

Trial contacts and locations

1

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Central trial contact

Lysha M Laurens

Data sourced from clinicaltrials.gov

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