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NCT06464354Completed

Comparison of the Mammary Harvesting Technique

Comparison of the Effect of Mammary Artery Harvesting Technique to Sternal Blood Supply Using Non-contact Dynamic Thermography

Source: ClinicalTrials.gov · Last updated 18 Jun 2024

Brief summary (registry, in English)

The skeletonization technique of left internal artery (LIMA) harvesting is reported as more spar-ing to the vascular supply of the sternum. Some studies report a greater length and greater flow of the graft additionally. The aim of our study was to measure the difference in post-op sternal blood supply compared to the pedicle harvesting technique and to measure the length and flow of the LIMA graft.

Status (registry)
Completed
Study type
Observational
Enrollment
90 (actual)
First submitted
12 Jun 2024
Start date
1 Jun 2023
Primary completion date
31 Dec 2023
Lead sponsor
University Hospital Ostrava
NCT number
NCT06464354

What you commit to

  • Study type: Observational
  • Participants enrolled: 90
  • From 1 Jun 2023 to the primary completion date, 31 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Emergent surgery

Other illness

  • Ongoing non-cardiac infection
  • Circulatory failure

Other

  • Re-operation
  • Re-sternotomy
  • Thoracotomy approach
  • Harvesting of both mammary arteries (BIMA)
  • Endocarditis
  • Fever
  • Ongoing administration of catecholamines to patient
  • Unsigned informed consent

Who the study is looking for

  • Elective cardiac surgery procedure via median sternotomy
  • The left mammary artery (LIMA) harvesting for coronary bypass planned as a part of the operation - Group 1 and 2
  • Other cardiac surgery procedures without the LIMA harvesting (valve surgery for instance) - Control group
  • Signing of the informed consent

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Ostrava
Coordinator of this site? Confirm its status
OstravaCzechiaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.