Peripheral Arterial Disease Trial, Recruiting NCT07322913 Sponsor: Intervascular Condition: Peripheral Arterial Disease
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Peripheral Arterial Disease Trial, Recruiting

NCT07322913
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 willing and able to sign a written consent form as required by the overseeing ethics or review board
  • People (male or female) who have had a surgery to bypass, replace, or repair blood vessels in the legs or arms, the main artery in the body (aorta), or the neck arteries (carotid arteries), using one of these specific graft or patch products: Intergard Standard, Hemashield, Intergard Silver, or Intergard Synergy
  • People who were at least 18 years old at the time of their surgery
  • People whose medical records are available and include at least 3 years of follow-up information after their surgery

Who may not be able to join:

  • People who had an active infection in the area where the graft or patch was placed at the time of their surgery (this applies specifically to the Intergard Standard and Hemashield products) (confirm with trial site)

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 28 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: Director, Clinical Affairs, Getinge

Phone: +1 603 233 7685

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
Intervascular
Registry
ClinicalTrials.gov
Start date
19 December 2025
Est. completion
1 December 2026

Where this trial is recruiting

🇫🇷 France 🇪🇸 Spain 🇺🇸 United States

Primary endpoints

Peripheral Arterial Disease Cohort: Cohort: Percentage of participants meeting primary device patency; Aortic Disease Cohort: Percentage of participants meeting primary device patency; Carotid Artery Disease Cohort: Percentage of participants achieving freedom from occlusion or reintervention; Peripheral Arterial Disease Cohort: Incidence of Major Adverse Limb Events (MALE); Aortic Disease Cohort: Incidence of Major Adverse Event (MAE); Devices with antimicrobial coating: Percentage of participants achieving freedom from infection; Carotid Artery Disease Cohort: Incidence of Major Adverse Even...

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: 28 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