Trials / Active Not Recruiting
Active Not RecruitingNCT06154265
Intraoperative Echocardiography in Low-Risk CABG Surgery
Default vs As-Needed Intraoperative Transesophageal Echocardiography (TEE) in Low-Risk Isolated Coronary Artery Bypass Graft (CABG) Surgery: A Randomized Controlled Trial
- Status
- Active Not Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- University of Pennsylvania · Academic / Other
- Sex
- All
- Age
- 18 Years – 100 Years
- Healthy volunteers
- Not accepted
Summary
This goal of this study is to better understand when and where intraoperative transesophageal echocardiography (TEE) should (or should not) be used during coronary artery bypass graft (CABG) surgeries.
Detailed description
This trial will look at benefits and harms to two different treatments strategies in order to improve clinical outcomes. Intraoperative TEE is an ultrasound-based, imaging device that uses sound valves to look at the heart continuously during a heart surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | TEE probe | Transesophageal echocardiography, ultrasound probe |
Timeline
- Start date
- 2024-01-22
- Primary completion
- 2025-03-15
- Completion
- 2025-12-31
- First posted
- 2023-12-04
- Last updated
- 2025-07-11
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06154265. Inclusion in this directory is not an endorsement.