Peripheral Arterial Disease Trial, Recruiting NCT06605209 Sponsor: Zhejiang Zylox Medical Device Co., Ltd. Condition: Peripheral Arterial Disease
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Peripheral Arterial Disease Trial, Recruiting

NCT06605209
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 aged 18 to 80 years, of any sex
  • People who have been diagnosed with a build-up of fatty deposits (atherosclerosis) in the main or outer iliac arteries, which are located in the pelvis and upper leg area
  • People whose leg symptoms fall within a specific range of severity, known as Rutherford classification 2 to 4, meaning symptoms ranging from mild pain during exercise to pain at rest (confirm with trial site)
  • People, or their legal representatives, who are able to understand the purpose of the study, follow the study rules, and sign a consent form

Who may not be able to join:

  • Women who are pregnant, planning to become pregnant, or currently breastfeeding
  • People who have previously had a vascular graft (an artificial tube used to bypass or repair a blood vessel) placed in their iliac artery
  • People who have had a stroke or heart attack within the 3 months before joining the trial
  • People with known bleeding or clotting disorders that cannot be corrected, or with blood test results showing seriously abnormal clotting levels or a very low platelet count
  • People whose kidney function is significantly reduced, based on a specific blood test result, or who are currently on dialysis
  • People with blood test results showing significantly elevated liver enzyme levels (ALT or AST more than twice the normal upper limit)
  • People with severe anaemia, meaning a very low red blood cell level (haemoglobin below 60.0 g/L)
  • People with known allergies or intolerances to certain materials or medications used in the study, including cobalt-based alloys, a type of synthetic graft material (ePTFE), aspirin, clopidogrel, heparin, rivaroxaban, paclitaxel, contrast dye, or other study-related substances
  • People who have had a vascular procedure within 30 days before the study surgery, or who plan to have one within 30 days after
  • People who have received a clot-dissolving treatment in the target blood vessel within 14 days before joining the trial
  • People with serious organ problems or other major health conditions that may affect their ability to follow the study rules, affect the results, or mean they are unlikely to complete the trial
  • People currently participating in another clinical trial involving an experimental drug, biological treatment, or medical device
  • People who the trial investigator considers unsuitable for any other reason

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

Phone: +86 010-66938349

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
Zhejiang Zylox Medical Device Co., Ltd.
Registry
ClinicalTrials.gov
Start date
8 November 2024
Est. completion
15 July 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

primary patency

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