Heart Diseases Clinical Trial
— TSTOfficial title:
Skeletonised Versus Pedicled Internal Thoracic Artery - A Randomised Study
Verified date | October 2022 |
Source | Odense University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
It is to date unknown whether Thunderbeat has a place in harvesting the left internal mammary artery (LIMA) and whether skeletonisation is superior to pedicle harvested LIMA. Though, some studies have shown improved flow-rates in the skeletonised graft while others shows compromised blood flow to the thoracic wall after pedicle harvested LIMA. The purpose of this study is to improve the quality of life for patients undergoing coronary artery bypass graft (CABG) operations. The aim of this study is to compare three groups of LIMA harvesting techniques: Pedicled, surgical skeletonised and skeletonised with Thunderbeat to determine the best way to harvest LIMA during CABG operations. The study design is an experimental randomized controlled trial in a single centre. Study population: Adult patients enlisted for elective stand-alone CABG surgery at the Department of Cardiothoracic surgery, Odense University Hospital. Study Unit: Test-days within subject and subject The study will address two main hypotheses in CABG patients: 1. That both the surgical skeletonised and Thunderbeat skeletonised harvesting techniques of LIMA are superior to pedicled harvesting in regards to flowrates and pulsatility index (PI). 2. Skeletonized harvesting of LIMA graft compared to pedicled harvesting improves patient quality of life three days, 30 days, and six months postoperatively.
Status | Completed |
Enrollment | 165 |
Est. completion date | November 30, 2021 |
Est. primary completion date | April 30, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Stand-alone CABG (surgical removal of the left atrial appendage (LAAX) is accepted, since it doesn't affect the graft area) - On-pump with cardioplegia (otherwise one cannot be sure of the pressure and perfusion during surgery of the graft) - Patients aged >18 - Elective surgery (there is a known higher risk of postoperative complications with urgent surgery) Exclusion Criteria: - CABG combined with other heart surgery, except from LAAX - Previous heart surgery - LVEF < 40% (there is a known higher risk of postoperative complications with low LVEF) - Known cancers (there is a known higher risk of postoperative complication) - Thoracic radiation therapy (there is a known higher risk of postoperative complication) - Severe chronic obstructive pulmonary disease (COPD) (there is a known higher risk of postoperative complication) - Patients not able to understand written consent - Urgent and emergent surgery (there is a known higher risk of postoperative complication) |
Country | Name | City | State |
---|---|---|---|
Denmark | Department of Cardio, Vascular and Thoracic Surgery | Odense | Region Of Southern Denmark |
Lead Sponsor | Collaborator |
---|---|
Lars Peter Riber | GCP-unit at Odense University Hospital, Odense Patient Data Explorative Network |
Denmark,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Differences in flow in LIMA and pulssatility index between the three groups. | mL/ min With transit time flowmetry (Sono TT flowlab), the graft flow and peripheral index (PI) are measured after weaning off the extracorporeal circulation with a systolic pressure aimed at 100 mmHg. The measurements are done with probe size 3 or 4. | Perioperative - After weaning off the extracorporeal circulation just before closing the thorax | |
Secondary | Postoperative bleeding | Unit: mL | Postoperative bleeding is measured from the end of the operation to removal of the mediastinal drains in the intensive care unit | |
Secondary | Re-operation due to bleeding | Number of patients in each group | Up to 48 hours calculated from the end of primaery surgery | |
Secondary | Re-operation due to ischemia | Number of patients in each group | Up to 48 hours calculated from the end of primaery surgery | |
Secondary | Pleurocentesis | Number of patients in each group | Up to 10 days calculated from the end of primaery surgery | |
Secondary | Myocardial injury - creatine kinase-MB (CK-MB) | Unit: (µg/L) | Routine bloodsample measured four hours after aortic cross clamp removal. | |
Secondary | Myocardial injury - cardiac troponin (cTn) | Unit: (ng/L) | Routine bloodsample measured four hours after aortic cross clamp removal. | |
Secondary | Differences in pre and post operative regional oxygen saturation on the thorax. | Unit: oxygen saturation (rSO2) | Measured 7 days prior to surgery and again 3 days after surgery | |
Secondary | Length of stay on ICU | Unit: Days | Day of surgery to the day of discharge from ICU. Up to 52 weeks | |
Secondary | Length of stay in hospital | Unit: Days | Day of surgery to the day of discharge from hospital. Up to 52 weeks | |
Secondary | EQ-5D-5L questionnaire: differences in self reported assessment of patient quality of life between the 3 groups | Developed by the EURO-QoF group in 1990 to describe five dimensions of quality of life: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has five levels: no problems, slight problems, moderate problems, severe problems and extreme problems and a visual analogue scale recording the patient's self-rated health. | Questionnaires uptained the week before the date of surgery and again 3, 30, and 180 days after surgery. | |
Secondary | Telephone interview - Questions regarding pain, numbness and wound healing around the thoracic incision. | All questions are closed questions and qualitative variables (yes/no) | 180 ± 7 days calculated from the date of surgery. | |
Secondary | Rate of readmission to hospital due to Major adverse cardiac and cerebrovascular events (MACCE) - early | Number of deaths in each group | Early (=30 days) | |
Secondary | Rate of readmission to hospital due to Major adverse cardiac and cerebrovascular events (MACCE) - Intermediate | Number of deaths in each group | Intermediate (=180 days) | |
Secondary | Rate of readmission to hospital due to Major adverse cardiac and cerebrovascular events (MACCE) - Long | Number of deaths in each group | Long (=2 years) | |
Secondary | Rate of mortality due to cardiac event - Early | Number of deaths in each group | Early (=30 days) | |
Secondary | Rate of mortality due to cardiac event - Intermediate | Number of deaths in each group | Intermediate (=180 days) | |
Secondary | Rate of mortality due to cardiac event - Iong | Number of deaths in each group | Long (=2 years) | |
Secondary | Rate of all-cause mortality - Early | Number of deaths in each group | Early (=30 days) | |
Secondary | Rate of all-cause mortality - Intermediate | Number of deaths in each group | Intermediate (=180 days) | |
Secondary | Rate of all-cause mortality - long | Number of deaths in each group | Long (= 2 years) |
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