Peripheral Arterial Disease Trial, Recruiting NCT06742801 Sponsor: Medtronic Endovascular Condition: Peripheral Arterial Disease
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Peripheral Arterial Disease Trial, Recruiting

NCT06742801
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are 22 years of age or older.
  • People who have active bleeding in blood vessels outside the brain and heart, confirmed by imaging (such as a scan or camera procedure), and where a procedure to block the bleeding vessel is considered appropriate by the treating doctor.
  • People who are able to provide written consent to take part, either personally or through a legally authorised representative.
  • People whose life expectancy is considered to be more than 30 days at the time of enrolling, in the opinion of the treating doctor.
  • People whose target treatment area has not previously been treated with an embolization procedure.

Who may not be able to join:

  • People who are pregnant or breastfeeding.
  • People who currently have signs or symptoms of an active infection.
  • People who are already taking part in another clinical trial involving an investigational drug, biological treatment, or medical device.
  • People who have an allergy to contrast dye, or another reason they cannot safely undergo angiography, CT scanning, or catheterisation, including contrast sensitivity that cannot be adequately managed before the procedure.
  • People who have a known allergy to the components of Onyx™ (the medical device used in this trial).
  • People whose blood vessels in the target treatment area are not considered suitable for delivery of Onyx™, based on the treating doctor's assessment.
  • People who, in the treating doctor's opinion after reviewing imaging, have more than four target areas that would require treatment.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Osman Ahmed, MD, University of Chicago

Phone: 7322662503

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Medtronic Endovascular
Registry
ClinicalTrials.gov
Start date
9 May 2025
Est. completion
1 April 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Freedom from Arterial Hemorrhage; Freedom from System-related Major Adverse Events (MAE)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov