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IVUS GUIDED for Coronary Heart Disease (IGT-PVI Trial)
N/A
Recruiting
Research Sponsored by Philips Clinical & Medical Affairs Global
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up procedure (one visit)
Awards & highlights
IGT-PVI Trial Summary
The main objective of the study is to survey and improve the IVUS image quality and X-ray system interoperability by collecting Procedural Data (e.g. raw, pre- processed ultrasound and X-ray data, endpoints such as fluoroscopy time, contrast load and radiation dose, workflow details) during routine intravascular procedures to assure adherence to the high standards of quality during care delivery and promote procedural standardization.
Eligible Conditions
- Coronary Heart Disease
- Peripheral Artery Disease
- Deep Vein Thrombosis
IGT-PVI Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ procedure (one visit)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~procedure (one visit)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Improve
Secondary outcome measures
PROCEDURAL AMOUNT OF CONTRAST USED
PROCEDURAL RADIATION DOSE
Procedural IVUS TIME
IGT-PVI Trial Design
1Treatment groups
Experimental Treatment
Group I: IVUS GUIDEDExperimental Treatment1 Intervention
Those undergoing an already planned IVUS guided treatment for percutaneous vascular interventions
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Who is running the clinical trial?
Philips Clinical & Medical Affairs GlobalLead Sponsor
49 Previous Clinical Trials
11,538 Total Patients Enrolled
Eric Secemsky, MDStudy ChairBeth Israel Deaconess Medical Center
1 Previous Clinical Trials
300 Total Patients Enrolled
Frequently Asked Questions
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