Contrast Volume Reduction During Percutaneous Coronary Interventions With the Use of a New Assisting Software Package
Status: Terminated
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY
The new software package is intended to assist the physician in imaging the coronaries during percutaneous coronary interventions. This study investigates the amount of contrast used during percutaneous coronary interventions with the aid of the new software package. The results of the study will be compared with control group data (before the new software package was installed or after it was removed) to define a possible contrast reduction.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Subject undergoing a percutaneous coronary intervention.
• Subject 18 years of age or older, or of legal age to give informed consent per state or national law.
Locations
United States
New York
Columbia University Medical Center/NYPH
New York
Time Frame
Start Date: 2017-12-15
Completion Date: 2019-06-30
Participants
Target number of participants: 80
Treatments
Study group
Percutaneous coronary interventions with additional imaging provided by the new software package
Control group
Percutaneous coronary interventions without the new software package
Authors
Related Therapeutic Areas
Sponsors
Leads: Philips Clinical & Medical Affairs Global