Effect of recently invented device in treatment of the angiography-induced pseudoaneurysm

A clinical trial to comparison the effectiveness of common ultrasound-guided with the recently invented device in treatment of the angiography-induced pseudoaneurysm

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190701044059N1

Enrollment

Registered

2019-07-14

Start date

2019-07-23

Completion date

Unknown

Last updated

2019-10-07

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

Conditions

The angiography-induced pseudoaneurysm. Aneurysm and dissection of artery of lower extremity

Interventions

Intervention 1: Intervention group: The intervention group will receive ultrasound-guided compression by the invented device. Intervention 2: Control group: The control group will ultrasound-guided co

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with pseudoaneurysm caused by angiography base on color Doppler ultrasound diagnostic criteria

Exclusion criteria

Exclusion criteria: Complete aneurysm block Complete thrombosis of the pseudoaneurysm Abscess, surface tissue infection, or open wound in the area History of angiography

Design outcomes

Primary

Measure	Time frame
Length, width and neck of pseudoaneurysm. Timepoint: Before and 6 hours after the intervention. Method of measurement: Ultrasound.	—

Secondary

Measure	Time frame
Pain levels. Timepoint: Before and 6 hours after the intervention. Method of measurement: Visual Analogue Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Kermani

Mashhad University of Medical Sciences

Z-k-65@yahoo.com+98 51 3840 0000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026