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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05931783
Other study ID # 1135/2023
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 12, 2024
Est. completion date October 1, 2031

Study information

Verified date June 2023
Source Medical University Innsbruck
Contact Hannes Abfalterer, Dr. med. univ.
Phone 004351250482988
Email hannes.abfalterer@i-med.ac.at
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Internal thoracic arteries can be harvested in skeletonized or pedicled technique. Latest research has posed a potential adverse effect of skeletonizing the internal thoracic arteries on graft patency rates and clinical outcome. Prospective, randomized, multi-centre trials are necessary to investigate the impact of harvesting technique of left internal thoracic artery (LITA) on graft patency rates and clinical outcome after coronary artery bypass grafting. The HARVITA trial compares skeletonized and pedicled harvesting technique of LITA regarding graft patency rates and patient survival.


Recruitment information / eligibility

Status Recruiting
Enrollment 1350
Est. completion date October 1, 2031
Est. primary completion date October 1, 2028
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion criteria: Primary isolated CABG patients with multi-vessel disease (defined as =70 % stenosis of the left anterior descending artery (LAD) and =50% stenosis of circumflex and right coronary territory, with or without a =50% stenosis of the left main artery). Exclusion criteria: - Age > 80 years - Planned CABG without LITA use - Preoperative mediastinal radiation therapy - Emergency operation - Minimal invasive coronary artery bypass surgery - Any concomitant cardiac or non-cardiac procedures - Previous cardiac surgery - Known contrast agent allergy - Severe stenosis of the left subclavian artery/ left-sided subclavian steal syndrome - Chronic kidney disease (GFR <60ml/min/1.73m²) - Life expectancy of less than 5 years - Pregnancy - Hyperthyroidism - Iodine allergy Intraoperative exclusion criteria: - Y/T graft off the LITA graft - LITA sequential grafting - LITA target vessel other than LAD

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
skeletonized harvesting technique
In patients who are randomized to this treatment arm, the left internal thoracic artery will be harvested in skeletonized technique. Thereby, only the artery itself is harvested.
pedicled harvesting technique
In patients who are randomized to this treatment arm, the left internal thoracic artery will be harvested in pedicled technique. Thereby, the artery will be harvested together with the accompanying veins, the endothoracic fascia and fatty tissue in order to create an 1-2 cm broad pedicle.

Locations

Country Name City State
Austria Medical University of Graz Graz
Austria Medical University of Innsbruck Innsbruck
Austria Medical University of Vienna Vienna
Germany University of Duisburg-Essen Essen
Germany University of Freiburg Freiburg
Germany University Hospital Gießen Gießen
Germany University of Jena Jena
Switzerland University Hospital Bern Bern

Sponsors (1)

Lead Sponsor Collaborator
Medical University Innsbruck

Countries where clinical trial is conducted

Austria,  Germany,  Switzerland, 

References & Publications (2)

Gaudino M, Audisio K, Rahouma M, Chadow D, Cancelli G, Soletti GJ, Gray A, Lees B, Gerry S, Benedetto U, Flather M, Taggart DP; ART Investigators. Comparison of Long-term Clinical Outcomes of Skeletonized vs Pedicled Internal Thoracic Artery Harvesting Techniques in the Arterial Revascularization Trial. JAMA Cardiol. 2021 Dec 1;6(12):1380-1386. doi: 10.1001/jamacardio.2021.3866. — View Citation

Lamy A, Browne A, Sheth T, Zheng Z, Dagenais F, Noiseux N, Chen X, Bakaeen FG, Brtko M, Stevens LM, Alboom M, Lee SF, Copland I, Salim Y, Eikelboom J; COMPASS Investigators. Skeletonized vs Pedicled Internal Mammary Artery Graft Harvesting in Coronary Artery Bypass Surgery: A Post Hoc Analysis From the COMPASS Trial. JAMA Cardiol. 2021 Sep 1;6(9):1042-1049. doi: 10.1001/jamacardio.2021.1686. Erratum In: JAMA Cardiol. 2021 Aug 18;:null. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Death or LITA graft occlusion in cCTA or invasive angiography within 2 years (+/- 3 months) after surgery. The primary endpoint will be compared between the two treatment groups using Kaplan-Meier graphs and a center stratified two sample log-rank test. In addition, Cox proportional hazards regression analysis adjusting for clinically relevant confounders will be performed. Hazard ratios and their 95% confidence intervals will be estimated.
LITA graft occlusion is defined as the absence of contrast detection in the lumen of the graft indicating a 100% occlusion of LITA graft.
2 years (+/- 3 months) after surgery
Secondary composite outcome of all-cause death, myocardial infarction and repeated revascularization The composite outcome of all-cause death, myocardial infarction and repeated revascularization will be compared with Kaplan-Meier graphs together with log-rank testing. 1 year, 2 years and 5 years after surgery
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