Indigo Aspiration System
Deviceuse of mechanical thrombectomy to treat pulmonary embolism
NCT Number: NCT03218566
To determine the safety and efficacy of the Indigo Aspiration System for aspiration mechanical thrombectomy in patients with acute pulmonary embolism (PE)
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Banner University Medical Center - Tucson, Tucson, Arizona, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
use of mechanical thrombectomy to treat pulmonary embolism
Time frame: from baseline to 48 hours
Change in RV/LV ratio per CTA
Time frame: within 48 hours
A composite of: device-related death, major bleeding, device-related SAEs (a composite of clinical deterioration, pulmonary vascular injury, cardiac injury)
Time frame: within 48 hours
Time frame: within 48 hours
Time frame: within 48 hours
Time frame: within 48 hours
Time frame: within 48 hours
Time frame: within 30 days
Time frame: within 30 days
Time frame: within 30 days
Penumbra Inc.
Industry
A Prospective, Multicenter Trial to Evaluate the Safety and Efficacy of the Indigo® Aspiration System in Acute Pulmonary Embolism
Acronym: EXTRACT-PE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06015529
Cardiovascular Diseases, Embolism
Brussels, Belgium
View Trial DetailsNCT04014972
Acute Aortic Syndrome, Aneurysm
View Trial DetailsNCT07689136
Cardiovascular Diseases, Deep Vein Thrombosis
Tunis, Tunisia
View Trial DetailsNCT06183944
Cardiovascular Diseases, Embolism
Toulon, France
View Trial Details