Outpatient Office Based Endovascular Procedures

The results of this study will serve as a starting point for future trials concentrating on the effectiveness and clinical outcomes of the procedures performed in an office based angiosuite. Additionally, other studies could compare clinical outcomes between procedures performed in an office based angiosuite and other settings.

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Key information

Conditions

Chronic Venous Insufficiency Arterial Occlusive Diseases Arterio-venous Fistula Arteriosclerosis Arteriovenous Fistula Arteriovenous Malformations Atherosclerosis Brain Diseases Brain Ischemia Cardiovascular Abnormalities Cardiovascular Diseases Central Nervous System Diseases Cerebrovascular Disorders Congenital Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities Dialysis Access Malfunction Fistula Nerve Compression Syndromes Nervous System Diseases Neuromuscular Diseases Pathological Conditions, Anatomical Pathological Conditions, Signs and Symptoms Peripheral Arterial Disease Peripheral Nervous System Diseases Peripheral Vascular Diseases Thoracic Outlet Syndrome Varicose Veins Vascular Diseases Vascular Fistula Vascular Malformations Vertebral Artery Insufficiency Vertebrobasilar Insufficiency

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Methodist Dallas Medical Center

Dallas, Texas, 75203, United States

About this study

Endovascular surgery combined with the demands of patients and physicians for less invasive procedures, have make this type of surgery one of the most innovative fields in medicine. However the endovascular experience in an office-based angiosuite is different from that in a hospital suite, and has been viewed in the past by some physicians as unsafe because it lacks the safety net of immediate hospital resources. In 2005, medicine allowed endovascular procedures to be performed in the office setting. The results of this study will serve as a starting point for future trials concentrating on the effectiveness and clinical outcomes of the procedures performed in an office based angiosuite.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Age ≥ 18 years.
Diagnosis of peripheral arterial disease (PAD), chronic venous insufficiency, dialysis access and malfunctioning arteriovenous fistulas, varicose veins, vertebrobasilar insufficiency, and thoracic outlet syndrome.
Procedures performed as an outpatient in an office based angiosuite.

Exclusion criteria

Age ≤ 18 years

Treatment and study plan

Primary outcomes

Discharge location

Time frame: April 2006 to December 2018

classified as home, hospital floor, ICU and emergency room.
postoperative complications

Time frame: April 2006 to December 2018

events that disrupted the normal recovery process of the patient within the 24 hours following the procedure

Sponsors and collaborators

Lead sponsor

Methodist Health System

Other

Registry information

Important dates

Study start: 2014
Primary completion: 2024
Study completion: 2024
First posted: Aug 13, 2019
Registry last updated: Mar 24, 2026

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.

Completed