Evaluation of Treatment Strategies for Severe CaLcIfic Coronary Arteries: Orbital Atherectomy vs. Conventional Angioplasty Technique Prior to Implantation of Drug-Eluting StEnts: The ECLIPSE Trial



Status:Recruiting
Conditions:Peripheral Vascular Disease, Cardiology, Cardiology, Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:4/5/2019
Start Date:March 27, 2017
End Date:December 31, 2021
Contact:Amber Dickson
Email:adickson@csi360.com
Phone:651-202-4135

Use our guide to learn which trials are right for you!

This trial will evaluate Orbital Atherectomy compared to conventional balloon angioplasty
technique for the treatment of severely calcified lesions prior to implantation of
drug-eluting stents (DES).


General Inclusion Criteria:

1. Subject is 18 years of age or older.

2. Subject presents with:

1. stable ischemic heart disease or

2. acute coronary syndrome (NSTEMI or unstable angina), or

3. stabilized recent STEMI (>48 hours prior to randomization procedure)

3. Subject has signed the Institutional Review Board (IRB) approved ECLIPSE trial
Informed Consent Form (ICF) prior to any trial related procedures.

General Exclusion Criteria

1. Subject has a history of any cognitive or mental health status that would interfere
with trial participation.

2. Subject is participating in or has plans to participate in any other investigational
drug or device trial that has not reached its primary endpoint.

3. Subject is a female who is pregnant.

4. Subject is receiving or scheduled to receive chemotherapy within thirty (30) days
prior or any time after the randomization procedure.

5. Subject has a life expectancy of ≤ 12 months.

6. Subject has undergone any prior PCI in the target vessel or its branches 12 months
prior to randomization.

7. Subject has undergone a PCI procedure that is unsuccessful or with complications
within 30 days prior to randomization, including during the randomization procedure.

8. Any cardiac intervention or surgery planned within 12 months post randomization
procedure aside from a potential planned staged PCI as part of the randomized
treatment strategy.

9. Subject has major valve disease and underwent intervention within 30 days prior to
randomization.

10. Subject has received a heart transplant.

11. Evidence of heart failure by at least one of the following (note - Left Ventricular
Ejection Fraction [LVEF] is not required by protocol):

1. Most recent LVEF ≤25%, or

2. Current heart failure defined as NYHA class ≥3 (all patients) or Killip class ≥2
(post STEMI patients)

12. Planned use in the randomized lesion(s) of a bare metal stent (BMS), bioresorbable
scaffold (BRS), non-stent treatment only.

13. Subject has a known sensitivity to contrast media, which cannot be adequately
pre-medicated.

14. Subject has a relative or absolute contraindication to aspirin or all P2Y12 inhibitor
agents, or will be unable to take both aspirin and a P2Y12 inhibitor for at least 6
months after PCI (e.g., due to a planned surgical procedure).

15. Subject has a history of a stroke or transient ischemic attack (TIA) within six (6)
months, or any permanent neurologic deficit.

16. Subject has a history of bleeding diathesis or coagulopathy or intention to refuse
blood transfusion if one should become necessary.

17. Subject has evidence of an active infection on the day of the randomization procedure
requiring oral or intravenous antibiotics.

18. Subject is not an acceptable candidate for emergent coronary artery bypass graft
(CABG).

19. Subject with known allergy to atherectomy lubricant components including soybean oil,
egg yolk phospholipids, glycerin and sodium hydroxide.
We found this trial at
100
sites
Carbondale, Illinois 62902
Principal Investigator: Raed Al-Dallow, MD
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1720 2nd Ave S
Birmingham, Alabama 35233
(205) 934-4011 
Principal Investigator: Mohammad Sarraf, MD
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75 Francis street
Boston, Massachusetts 02115
(617) 732-5500
Principal Investigator: Kevin Croce, MD
Brigham and Women's Hosp Boston’s Brigham and Women’s Hospital (BWH) is an international leader in...
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9500 Euclid Avenue
Cleveland, Ohio 44106
216.444.2200
Principal Investigator: Jaikirshan Khatri, MD
Cleveland Clinic Cleveland Clinic is committed to principles as presented in the United Nations Global...
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425 University Blvd.
Indianapolis, Indiana 46202
(317) 274-4591
Principal Investigator: Ziad Jaradat, MD
Indiana University INDIANA UNIVERSITY is a major multi-campus public research institution, grounded in the liberal...
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8700 Beverly Blvd # 8211
Los Angeles, California 90048
(1-800-233-2771)
Principal Investigator: Suhail Dohad, MD
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24 Sturtevant St
Orlando, Florida 32806
Principal Investigator: Mark Steiner, MD
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22 Bramhall St
Portland, Maine 04102
(207) 662-0111
Principal Investigator: Samip Vasaiwala, MD
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593 Eddy Street
Providence, Rhode Island 02903
401-444-4000
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Seattle, Washington 98104
(206) 543-2100
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Tampa, Florida 33607
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Albany, New York 12208
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500 S State St
Ann Arbor, Michigan 48109
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Atlanta, Georgia 30309
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303 Parkway Drive Northeast
Atlanta, Georgia 30033
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Birmingham, Alabama 35205
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130 S Bryn Mawr Ave
Bryn Mawr, Pennsylvania 19010
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41 Mall Road
Burlington, Massachusetts 1805
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3555 South Val Vista Drive
Chandler, Arizona 85224
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Chapel Hill, North Carolina 27599
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4500 S. Lancaster Rd.
Dallas, Texas 75216
800-849-3597
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6401 France Ave S
Edina, Minnesota 55435
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743 Spring St NE
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3535 Southern Blvd
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9500 Gilman Dr
La Jolla, California 92093
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2160 South 1st Avenue
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2900 W Oklahoma Ave
Milwaukee, Wisconsin 53215
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20 York St, N20 York St,
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1514 Jefferson Highway
New Orleans, Louisiana 70121
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450 Lakeville Road
New York, New York 11042
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4440 West 95th Street
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320 E North Ave
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1 Shields Ave
Sacramento, California 95616
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1406 6th Avenue North
Saint Cloud, Minnesota 56303
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5300 Tallman Ave NW
Seattle, Washington 98122
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