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Clinical Trials/NCT04796493
NCT04796493Active, not recruitingNot Applicable

Is Objective Grading of Mesenteric Traction Syndrome With Laser Speckle Contrast Imaging Interchangeable With Digital Thermography

Rigshospitalet, Denmark1 site in 1 country98 target enrollmentStarted: March 16, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
98
Locations
1
Primary Endpoint
Severity of MTS - measured facial perfusion

Study Overview

Brief Summary

Mesenteric traction syndrome (MTS) is defined as hypotension, tachycardia and facial flushing in the first hour of surgery, caused by mesenteric traction/abdominal exploration. MTS occurs frequently during abdominal surgery, with incidence around 80 % during open surgery, and lower during minimally invasive surgery. MTS can be divided into different severities using the degree of facial flushing, with the most severe level of MTS being associated with increased postoperative morbidity.

Today MTS is diagnosed and graded subjectively by the surgical team, with marked difficulty and limitations. Therefore the investigators developed a cut-off value using the Laser Speckle Contrast Imaging (LSCI), which the investigators wish to confirm in a new cohort, while also examining whether LSCI is interchangeable with digital thermography, which is simpler and cheaper to perfom.

The investigators will measure facial perfusion during the first hour of surgery and take blood samples at predefined timepoints to use for biochemical verification of the different severities of MTS.

Three cohorts we planned to include 45 open esophagectomies or gastrectomies 50 whipple surgery 20 robot assisted esophagectomies or gastrectomies These patients will be use in multiple articles examining different aspects of MTS

One study examining LSCI and thermography for the identification and grading of MTS will use 60 patients undergoing open esophagectomy or gastrectomy or whipple surgery, in this study patients will not be excluded if they are found to be disseminated.

However we ended up including 37 open esophagectomies - due to few patients undergoing open esophagectomy, this were included over a time period of almost 2,5 years 50 whipple 11 Robotic esophagectomies - due to LSCI being impossible to use on robotic esophagectomies and thermography being diffciult to fit on these patients and as such not being feasible

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Undergoing curative surgery for esopageal, gastric, doudenal or pancreatic cancer

Exclusion Criteria

  • •Known flushing disease
  • •Patients recieving NSAID and corticosteroid presurgery, Whipple is allowed to recieve single dose of 125 mg Methylprednisone as part of the standard of care at our facility.
  • •Palliative surgery
  • •Surgery not completed due to disseminated disease - patients will still be used in examination of LSCI and Thermography analysis even if desiminated

Outcomes

Primary Outcomes

Severity of MTS - measured facial perfusion

Time Frame: first hour of surgery

Facial perfusion measured with LSCI and Digital Thermography

Secondary Outcomes

  • Markers of postoperative impact of MTS - IL6 and endothelial damage markers(During and after surgery)
  • Biochemical markers of MTS - prostacyclin(During surgery)
  • Incidence of objective MTS during minimally invasive surgery(during surgery)
  • Hemodynamics(During surgery)
  • 30-day postoperative morbidity(30 days post surgery)
  • PACU - length of stay(At the PostAnesthesia Care Unit following surgery. Typically one to two days)
  • Incidence of objective MTS during whipples procedure with methylprednisolone prophylaxis(During surgery)
  • PACU - vasopressor requirements(At the PostAnesthesia Care Unit following surgery.Typically one to two days)
  • suPAR (soluble urokinase Plasminogen Activator Receptor).(baseline just prior to surgery)
  • PACU - fluid therapy administred at PACU(At the PostAnesthesia Care Unit following surgery. Typically one to two days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

August Adelsten Olsen

MD PhD student

Rigshospitalet, Denmark

Study Sites (1)

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