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Evaluation of Glycocalyx in Major Abdominal and Thoracic Surgery

Prospective Observational Study to Evaluate Glycocalyx Alteration in Major Abdominal and Thoracic Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04900779
Enrollment
117
Registered
2021-05-25
Start date
2021-02-02
Completion date
2022-05-31
Last updated
2021-05-25

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

Conditions

Major Elective Abdominal and Thoracic Surgery

Brief summary

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.

Interventions

None listed

Sponsors

Hospital Universitari Vall d'Hebron Research Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
plasmatic syndecan -1 levelsIn the first 24 hours after the procedureDegradation of glucocalix measured by plasmatic syndecan -1 levels

Countries

Spain

Contacts

Primary ContactLysha M Laurens
michelle.laurens.a@gmail.com+34698209872

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026