MAGIC-PAD Trial

Multicenter Aggressive wire recanalization in calcified atheroma and dilatation technique for GIant Calcified lesion in Peripheral Artery Disease trial

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-jRCT1020220033

Enrollment

200

Registered

2022-11-29

Start date

2022-11-29

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

arteriosclerosis obliterans

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)18 years of age or older 2)Peripheral artery disease with de novo Iliac/CFA/SFA/PopA eccentric calcified lesion>= 75% 3)Patients with an indication for EVT 4)Patients with accessible medical records throughout the observation term 5)Patients have provided written informed consent

Exclusion criteria

Exclusion criteria: 1)Inability to provide written informed consent 2) Life expectancy less than 12 months 3)Estimated high risk of non-availability for antiplatelet or anticoagulant medications 4)Patients with other reasons inappropriate for inclusion in the study

Design outcomes

Primary

Measure	Time frame
Primary patency at 12 & 24 months	—

Secondary

Measure	Time frame
1)Minimum lumen diameter 2)Eccentricity index of the target lesion 3)Change in Ankle-Brachial Index before and after EVT 4)Technical success rate of ARCADIA technique 5)Ankle-Brachial Index at 12 and 24 months 6)Rutherford class at 12 and 24 months 7)Procedural complications 8)Procedural time, fluoroscopy time, radiation dose, Contrast volume 9)Minimum lumen diameter by contrast CT at 12 and 24 months (Iliac only)	—

Measure

Time frame

1)Minimum lumen diameter 2)Eccentricity index of the target lesion 3)Change in Ankle-Brachial Index before and after EVT 4)Technical success rate of ARCADIA technique 5)Ankle-Brachial Index at 12 and 24 months 6)Rutherford class at 12 and 24 months 7)Procedural complications 8)Procedural time, fluoroscopy time, radiation dose, Contrast volume 9)Minimum lumen diameter by contrast CT at 12 and 24 months (Iliac only)

—

Contacts

Public ContactHirokazu Konishi

Tokyo Metropolitan Tobu Chiiki Hospital, Tokyo Metoropolitan Hospital Organization

h-kony0408@ozzio.jp+81-3-5682-5111

Outcome results