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NCT01444378 · ClinicalTrials.gov registry record · NA

Absolute Pro® MOMENTUM™

A NA study of Peripheral Artery Disease and Peripheral Vascular Disease, sponsored by Abbott Medical Devices.

Completed
Registry status
NA
Development phase
141
Enrollment target
1
Study location

NCT01444378 is a NA study of Peripheral Artery Disease and Peripheral Vascular Disease that has completed, run by Abbott Medical Devices. The registered enrollment target is 141 participants, above the 124-participant average among 50 other Peripheral Artery Disease trials with a reported enrollment target (14% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT01444378, a NA study of Peripheral Artery Disease and Peripheral Vascular Disease, has completed, sponsored by Abbott Medical Devices.

COMPLETED
Registry status
NA
Development phase
141 participants
Enrollment target
1
Study location

Study Summary

To evaluate the safety and effectiveness of the Absolute Pro® Peripheral Self-Expanding Stent System and the Absolute Pro® LL Peripheral Self-Expanding Stent System for the treatment of subjects with atherosclerotic de novo or restenotic lesions in the native superficial femoral artery (SFA) and/or the native proximal popliteal artery (PPA). CAUTION: Absolute Pro® Peripheral Self-Expanding Stent System and the Absolute Pro® LL Peripheral Self-Expanding Stent Systems are investigational devices. Limited by Federal (U.S.) law to investigational use only.

Interventions

  • DEVICE Stenting using Absolute Pro® and Pro LL® Peripheral Stent Systems

Study Locations (1)

California

  • Abbott Vascular - Santa Clara

Trial Details

FieldValue
Enrollment Target 141 participants
Start Date 2011-10
Est. Completion 2015-05
Phase NA

Sponsor

Abbott Medical Devices

261 total trials

What the Registry Record Tells You About NCT01444378

The ClinicalTrials.gov registry entry for NCT01444378 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 141 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 124-participant average among 50 other Peripheral Artery Disease trials with a reported enrollment target (14% higher). The listed sponsor is Abbott Medical Devices, which has 261 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Peripheral Artery Disease appearing as the primary indexed condition, and to 1 intervention - of which Stenting using Absolute Pro® and Pro LL® Peripheral Stent Systems is the first listed.

NCT01444378 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT01444378 about?

NCT01444378 is a clinical study titled "Absolute Pro® MOMENTUM™". To evaluate the safety and effectiveness of the Absolute Pro® Peripheral Self-Expanding Stent System and the Absolute Pro® LL Peripheral Self-Expanding Stent System for the treatment of subjects with atherosclerotic de novo or restenotic lesions in the native superficial femoral artery (SFA) and/or ...

What is the current status of trial NCT01444378?

This trial is currently completed. It is a NA study. The enrollment target is 141 participants. The study started on 2011-10. Estimated completion is 2015-05.

What conditions does trial NCT01444378 study?

This clinical trial studies the following conditions: Peripheral Artery Disease, Peripheral Vascular Disease.

What interventions are being tested in trial NCT01444378?

The interventions under investigation include: Stenting using Absolute Pro® and Pro LL® Peripheral Stent Systems (DEVICE).

Who is sponsoring clinical trial NCT01444378?

This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01444378 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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