I25.9
Conditions
Interventions
Group 1: Thoracoscopic harvesting of the mammary artery. Within the scope of this study, specific examinations and assessments are performed at defined time points. Pulmonary function testing is condu
Sponsors
Universitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patients with coronary heart disease 2. Consent of the patient after detailed explanation of the study being conducted 3. Patients with coronary heart disease and surgical findings that can be treated with minimally invasive bypass surgery
Exclusion criteria
Exclusion criteria: 1. Preoperative Forced Expiratory Volume in 1 Second 35 3. Patient lacks capacity to give consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| • Postoperative pain determined using the pain scale (1-10) • Lung function (Forced Expiratory Volume in 1 Second, Vital Capacity and Diffusing Capacity of the Lung for Carbon Monoxide) • Length of hospital stay | — |
Secondary
| Measure | Time frame |
|---|---|
| • Duration of surgery • Length of stay in intensive care • Postoperative troponin levels • Neurological symptoms affecting the arm • Hemothorax and postoperative bleeding | — |
Countries
Germany
Contacts
Public ContactFarhad Bakhtiary
Universitätsklinikum Bonn
Outcome results
None listed