Cardiac Complication

2

Review clinical trials related to Cardiac Complication. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Registry for the Improvement of Postoperative OutcomeS in Cardiac and Thoracic surgEry

The registry for the improvement of postoperative outcomes in cardiac and thoracic surgery aims to prospectively collect data in order to test the association between various preoperative and per-operative variables ; and several postoperative outcomes such as mortality, shock, redo surgery, sepsis and extracorporeal life-support.

Participants needed: 8,000
Trial details
Biological sex: AllType: ObservationalSponsor: CMC Ambroise ParéUpdated: Apr 3, 2026Locations: 1Duration: 2 Months
Eligibility criteria

all patients eligible for cardiac or thoracic surgery

non applicable

Status: Recruiting

Femoral Arterial Cannulation in Pediatrics

The goal of this clinical trial\] is to evaluate the efficacy and safety of the ultrasound-guided "Modified Dynamic Needle Tip Positioning Short-Axis, Out-Of-Plane" (MDNTP-SAOP) technique compared to the "Conventional, Short-Axis, Out-Of-Plane" (C-SAOP) technique for femoral arterial cannulation performed by anesthesia residents in children. The main question it aims to answer is: What is the time required for attempted femoral arterial cannulation by anesthesia residents at the first puncture site? Researchers will compare the efficacy and safety of MDNTP-SAOP versus C-SAOP methods for femoral arterial cannulation performed by anesthesia residents in infants and children undergoing cardiac surgery. Participants will be randomized to either the MDNTP-SAOP or the C-SAOP group. Intraoperatively, time taken for attempted cannulation by the resident at the first site of femoral arterial puncture, number of attempts at arterial cannulation, and number of cannulae required for successful cannula insertion will be recorded. Adverse events will be monitored on postoperative days 1 and 3. The insertion site will be examined for thrombosis, hematoma, infection, or limb ischemia distal to the insertion site

Participants needed: 80
Trial details
Age: Up to 12Biological sex: AllType: InterventionalSponsor: American University of Beirut Medical CenterUpdated: Jul 20, 2025Locations: 1
Eligibility criteria

Infants and children under 12 years of age. [+2]

Need for emergency surgery. [+1]