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Glycocalyx Monitoring in Major Abdominal Surgery

Evaluation of Perioperative Glycocalyx Monitoring in Major Abdominal Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06285526
Acronym
GLYCOCHIP
Enrollment
78
Registered
2024-02-29
Start date
2022-07-05
Completion date
2026-05-13
Last updated
2026-05-22

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

Conditions

Major Abdominal Surgery

Keywords

Glycocalyx, Microcirculation, Cephalic DuodenoPancreatectomy, Hyperthermic Intraperitoneal Chemotherapy

Brief summary

The study of the microcirculation and glycocalyx could be an essential element in the monitoring of our patients undergoing major abdominal surgery. It would enable us to better target the objectives of anaesthesia and resuscitation, which until now have been based essentially on macro-circulatory parameters.

Detailed description

This monitoring is possible in real time and real conditions by micro-camera GlycoCheck™ (Microvascular Health Solutions Inc., Salt Lake City, Utah, USA), a non-invasive monitoring allowing the study of sublingual microcirculation and glycocalyx.

Interventions

PROCEDURECytoreduction surgery with Hyperthermic Intraperitoneal Chemotherapy

Cytoreduction surgery with Hyperthermic Intraperitoneal Chemotherapy

PROCEDURECephalic DuodenoPancreatectomy

Cephalic DuodenoPancreatectomy

Sponsors

University Hospital, Rouen
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years

Inclusion criteria

For the HIPEC group : * Adult patients * Age \< 75 years * Receiving HIPEC for primary or secondary peritoneal carcinosis For the CDP group : * Adult patient * Age \< 75 years * Receiving CDP for pancreatic neoplasia * Patient who has read and understood the information letter and does not object to taking part in the study * Patient affiliated to a social security scheme

Exclusion criteria

* Secondary distant peritoneal metastases * Chronic heart failure * Chronic liver failure at stage C of the Child-Pugh score * Stage IV or V chronic renal failure * Inflammation of the sublingual buccal mucosa or injury that may locally influence sublingual microcirculation * Patient refusal * Person deprived of liberty by an administrative or judicial decision or person placed under court protection or guardianship

Design outcomes

Primary

MeasureTime frameDescription
Glycocalyx thicknessbetween the day before the operation (Day -1) and the post-operative period (Day 1)Perioperative variation in glycocalyx thickness (µm)

Secondary

MeasureTime frameDescription
Glycocalyx thickness and a biological marker of tissue hypoperfusionpost-operative period (Day 1)To assess, in each population ((HIPEC and CDC), the association between the thickness of the glycocalyx established by analysis of the sublingual microcirculation using GlycoCheck® and a biological marker of tissue hypoperfusion.
Glycocalyx thickness and a biological marker of tissue hypoxiapost-operative period (Day 1)Establish the link between glycocalyx thickness and a biological marker of tissue hypoxia.
Blood cell velocity and macrocirculatory functionpost-operative period (Day 1)Assess the association between velocity of the red blood cells (µm/s) and cardiac index obtained by Most-Care® monitoring on Day 1.
Perfused capillary density and macrocirculatory functionpost-operative period (Day 1)Assess the association between perfused capillary density (mm/mm2) and cardiac index obtained by Most-Care® monitoring on Day 1.
Variation of glycocalyx thickness and the daily entry-exit balance (BES) Day 1between Day -1 and Day 1To assess the difference between water and fluid intake (perfusion, nutrition, drug dilution solution) and output (diuresis, digestive aspiration, diarrhoea) over 24 hours

Countries

France

Contacts

PRINCIPAL_INVESTIGATORZoé DEMAILLY, Dr

University Rouen Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026