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OEIS Outcome Data Registry

OEIS (Outpatient Endovascular and Interventional Society) Outcome Data Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03058913
Enrollment
600000
Registered
2017-02-23
Start date
2017-02-01
Completion date
2025-12-31
Last updated
2022-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Peripheral Arterial Disease

Brief summary

This registry is created under the sponsorship of the Outpatient Endovascular and Interventional Society (OEIS) to monitor the clinical course and treatment outcomes of patients undergoing office-based endovascular procedures.

Interventions

None listed

Sponsors

Syntactx
CollaboratorNETWORK
Outpatient Endovascular and Interventional Society
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient is 18 years of age or older; * Patient is identified as having undergone a percutaneous transluminal vascular intervention or attempted intervention, in an ambulatory (outpatient) facility, for the treatment of peripheral vascular disease within native arteries or bypass grafts, from the infrarenal aorta distally to the feet.

Exclusion criteria

* Patient treated for a non-eligible condition or procedure * Diagnostic procedures without intervention or attempted interventions * Serious mental illness that might preclude subject's ability to comply with follow up * Life expectancy of less than 6 months

Design outcomes

Primary

MeasureTime frameDescription
Antiplatelet Therapy (ACC/AHA/PAD Coalition)30 daysTo collect the clinical variables of Patients undergoing endovascular procedures in an outpatient angiograPercentage of patients with PAD that have been prescribed an antiplatelet medication at the reported encounter.
Preventive Care and Screening: Tobacco Use30 daysScreening and Cessation Intervention. Percentage of patients aged 18 years and older who were screened for tobacco use one or more times within 24 months AND who received cessation counseling intervention if identified as a tobacco user.
Lipid-Lowering Medications for Patients with PAD30 daysThe rate at which patients with documented peripheral artery disease have documentation of a currently prescribed antihyperlipidemic medication treatment. This may include one of the following: Statin, Bile acid sequestrants, Niacin, Ezetemibe, Fibrates, PCSK9 Inhibitors
Optimal vascular care30 daysThis measure is a composite score of appropriate vascular care measures for treatment of PAD. This measure is a composite result of 1: Antiplatelet Therapy; 2: Preventive Care and Screening: Tobacco Use; and 3: Lipid-Lowering Medications (Statin) for Patients with PAD
Preventive Care and Screening: Influenza Immunization.30 days
Pneumonia Vaccination Status for Older Adults.30 days
Preventive Care and Screening: Screening for High Blood Pressure and Follow-Up Documented.30 days
Appropriate non-invasive arterial testing for patients with intermittent claudication who are undergoing a lower extremity peripheral vascular intervention.30 daysProportion of patients with non-invasive evaluations present/available prior to lower extremity peripheral vascular interventions in patients with intermittent claudication.
Appropriate non-invasive arterial testing for patients with critical limb ischemia who are undergoing a LE peripheral vascular intervention.30 daysProportion of patients with non-invasive evaluations present/available prior to LE peripheral vascular interventions in patients with critical limb ischemia.
Emergent transfer from an outpatient, ambulatory surgical center, or office setting.30 daysRate of emergent transfer from an outpatient, ASC, or office setting to an acute care facility as a result of an invasive peripheral vascular intervention.

Countries

United States

Contacts

Primary ContactDhru Bhatt
DBhatt@association-resources.com8885486347
Backup ContactElizabeth Ouriel
eouriel@syntactx.com2128786882

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026