Skip to main content
OpenTrials
Completed

NCT Number: NCT03267056

AcoArt IV / SFA in China:Drug-eluting Balloon for SFA Angioplasty Evaluation in China

The registry is a prospective, multicenter, single arm post-market real-world registry in China assessing the clinical use, safety and outcomes of the Orchid 035 DCB Catheter in the Superficial Femoral Artery (SFA) and Popliteal Arteries (PA).

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Chinese PLA General Hospital, Beijing, Beijing Municipality, China

Loading trial locations.

About this study

PTA is an established alternative to open surgical bypass for the treatment of infrainginual disease of critical limb ischemia.

DEBs are designed to promote arterial patency by reducing neointimal proliferation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 18 and 80 years
  • Patients with peripheral artery disease (PAD), with Rutherford classification between 2 and 5
  • an occlusion or a minimum grade of stenosisPrimary over 70% in the superficial femoral artery an /or the popliteal artery
  • Total length of treat lesion(s)is less or equal to 20cm
  • signed Patient informed consent form

Exclusion criteria

  • plasma Cr level greater than 150 umol/L in patients
  • patients with acute thrombosis requiring lysis or thrombectomy
  • 2 or more than 2 stenosis lesions in traget vessel
  • patient with a lysis or an lower limb intervention as a therapy within the last 6 weeks
  • patient requiring intervention in both lower limbs at the same time
  • have >30% residual stenosis or blood-limited dissection after predilation
  • distal outflow through less than one lower leg vessel
  • known hypersensitivity to aspirin, heparin, clopidogrel,paclitaxel, contrast medium, etc.
  • patients participating in another clinical trials with interfere with this trial in the past 3 months
  • pregnancy and lactating woman
  • untreatable bleeding diatheses
  • other diseases, such as cancer, liver disease, or cardiac insufficiency, which may lead to protocol violations or markedly shorten a patients's life expectancy(less than 1 years)
  • patients unable or unwilling to participate this trial

Treatment and study plan

drug eluting balloon catheter (trade name: Orchid)

Device

use drug eluting balloon catheter(trade name: Orchid) to inflate the stenosis or occlusion in superficial femoral artery(SFA) and/or popliteal artery

Primary outcomes

  1. Primary patency of target lesion.

    Time frame: 12 months

    The primary efficacy end point was primary patency at 12 months following the index procedure, defined as freedom from clinically driven target lesion revascularization and restenosis as determined by a duplex ultrasonography-derived peak systolic velocity ratio of

    ≤2.4

Secondary outcomes

  1. target lesion revascularization,target lesion revascularization is defined as any reintervention of artery bypass graft surgery involving the target lesion

    Time frame: 6 months, 12 months

    target lesion revascularization is defined as any reintervention of artery bypass graft surgery involving the target lesion

  2. improvment in Rutherford stage

    Time frame: 6 months, 12 months

    improvementin Rutherford stage is defined as an upward shift of at least 1 category on Rutherford classification as compared to baseline

  3. change in ankle brachial index(ABI)

    Time frame: 12 months

    change in ankle brachial index(ABI) compared to baseline

  4. Device success during the operation

    Time frame: during the operation

    Device success is defined as successful delivery, balloon inflation, deflation and retrieval of the intact study device without burst below the rated burst pressure (RBP).

Sponsors and collaborators

Lead sponsor

Acotec Scientific Co., Ltd

Industry

Registry information

Official study title

Real-World Registry Assessing the Clinical Use of the Orchid Drug Coated Balloon Catheter

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Aug 30, 2017
Registry last updated
Aug 19, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.