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Status unknownNCT03452904FADDYUpdated Mar 23, 2018

FrActional Flow Reserve Guided Drug Coated Balloon Only Strategy in De Novo coronarY Lesions (FADDY)

A Phase 3 interventional study of Drug-coated balloon and Drug-eluting stent in Coronary Stenosis, sponsored by Second Affiliated Hospital, School of Medicine, Zhejiang University. Status unknown at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-03-23.

Sponsored by Second Affiliated Hospital, School of Medicine, Zhejiang University · Phase 3, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2017), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 3
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Drug-eluting stent (DES) has been the primary choice for in suit coronary lesions treatment. In comparison to bare-metal stent (BMS), it evidently decreases the rate of restenosis. However, in recent years in-stent restenosis or thrombogenesis caused by acquired stent malapposition in the late stage or by new in-stent atherosclerotic plaques was oberved, which possibly was associated with chronic inflammation stimulation because of residual intravascular metal or polymer coating. Through being expanded around 30 to 60 seconds, drug-coated balloon (DCB) can ensure adequate paclitaxel enter the artery wall, which can inhibit smooth muscle cells hyperplasia without remaining any foreign body. In recent small sample trials, they showed that sole DCB treatment had a good long-term effect when pre-treating ideal in suit coronary lesions (defined as residual stenosis\< 30%, without dissection severer than type C, anterograde flow TIMI III). In PEPCAD I trial, the rate of major adverse cardiovascular events (MACE) was 6.1% in the first 12 months and persistent to 3-year follow up. Small sample prospective observational study from Korea, like Shin, showed that in the in suit coronary lesions with the fractional flow reserve (FFR)>0.85 after percutaneous transluminal coronary angioplasty (PTCA), the FFR kept unchanged in the 9-month follow up after DCB treatment and there was not MACE happened. However, so far randomized controlled trials with large sample to confirm their non-inferiority compared with DES when treating relatively larger in suit coronary lesions are lacked. Meanwhile, a number of doctors worried about acute cardiovascular occlusion and long-term restenosis. In this study, we assume that in the in suit coronary lesions with FFR>0.85 after PTCA pre-treatment, DCB treatment is not inferior to DES treatment regarding to middle- and long-term functional recovery.

02

Conditions studied

  • Coronary Stenosis

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Keywords

  • In suit coronary lesions
  • Drug-coated balloon
  • Drug-eluting stent
  • Restenosis
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Clinical Criteria:

    1. Patients with age >= 18 years old
    2. Patients with coronary artery disease is confirmed by angiography
    3. Patients with angina (CCS class II-IV) or documented ischemia evidence with ECG or ECT
    4. Patients agree to sign the informed consent
  • Angiographic Criteria:

    1. In suit coronary lesions
    2. Reference diameters of target vessels by visual estimation from 2.5 mm to 3.5 mm and \< 28 mm in length
    3. Lesion diameter stenosis >= 70% by visual estimation or >= 50% with objective ischemia evidence (exercise stress testing, ECT or FFR\< 0.8)

Exclusion criteria

Exclusion Criteria:

  • Clinical Criteria:

    1. Patients with STEMI \<= 1 week
    2. Patients with LVEF \< 30%
    3. Patients with bleeding diathesis or known anticoagulation dysfunction
    4. Patients with medical history regarding of intracranial tumor, aneurysm, arteriovenous malformation or cerebral apoplexy; stroke or TIA within 6 months; gastrointestinal hemorrhage within 2 months; major surgery within 6 weeks; recent or known platelet \< 100,000/mm3 or hemoglobin \< 10 g/dL
    5. Patients with planed selective operation probably leading to stopping using ADP receptor antagonists in advance
    6. Patients with life expectancy is less than 1 year because of combined comorbidity of other system
  • Angiographic Criteria:

    1. Acute thrombotic lesions
    2. Left main coronary artery lesions
    3. Severe intima tear lesions
    4. Coronary artery bypass grafts lesions
    5. In-stent restenosis
04

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Drug-coated balloon

    Treatment of in suit coronary lesions with drug-coated balloon

    Device: Drug-coated balloon

  • Active comparator
    Drug-eluting stent

    Treatment of in suit coronary lesions with drug-eluting stent

    Device: Drug-eluting stent

Interventions

  • DeviceDrug-coated balloon

    Treatment of in suit coronary lesions with drug-coated balloon

  • DeviceDrug-eluting stent

    Treatment of in suit coronary lesions with drug-eluting balloon

05

What researchers measure

Primary outcomes

  1. 9-month fractional flow reserve value

    Time frame: 9 months

Secondary outcomes

  1. Late lumen loss

    Time frame: 9 months

  2. Percent restenosis

    Time frame: 9 months

  3. Failure rate of target lesions

    Time frame: 9 months

  4. Rate of thrombosis in target lesions

    Time frame: 9 months

  5. Cumulative MACE rate

    Time frame: 9 months

  6. Success rate of the strategy

    Time frame: 9 months

06

Study locations

1 of 1 sites recruiting
  • Second Affiliated Hospital Zhejiang University School of Medicine
    Hangzhou, Zhejiang 310009, China
    • Jun Jiang, MD,PhD · Contact · drjayj@hotmail.com · +86-13588706891
    • Jian-an Wang, MD,PhD · Principal investigator
    Recruiting
07

Registry details

Key details

Study ID
NCT03452904
Lead sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Collaborators
Ningbo No. 1 Hospital
Responsible party
Sponsor
First posted
Mar 2, 2018
Start date
Jan 2017
Primary completion
Sep 2018 (estimated)
Completion
Sep 2018 (estimated)
Last update
Mar 23, 2018

Study contacts

Jun Jiang, MD,PhD
Contact
drjayj@hotmail.com
+86-13588706891
Jian-an Wang, MD,PhD
Contact
Wang_jian_an@tom.com
+86-13805786328
Jian-an Wang, MD,PhD
study chair · Second Affiliated Hospital of Zhejiang University, School of Medicine

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.

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