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NCT05755711Active, not recruiting

Equity in Modifying Plaque Of WomEn With UndeRtreated Calcified Coronary Artery Disease

Source: ClinicalTrials.gov · Last updated 30 Jul 2026

Brief summary (registry, in English)

Post-market, prospective, multi-center, single-arm observational study to generate real-world clinical evidence associated with coronary IVL in a population of female subjects with calcified coronary artery disease.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
399 (actual)
First submitted
21 Feb 2023
Start date
3 May 2023
Primary completion date
11 Dec 2024
Lead sponsor
Shockwave Medical, Inc.
NCT number
NCT05755711

What you commit to

  • Study type: Observational
  • Participants enrolled: 399
  • From 3 May 2023 to the primary completion date, 11 Dec 2024
  • 49 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Serious angiographic complication in the target vessel prior to treatment with coronary IVL including-severe dissection (Type D to F), perforation, abrupt closure, persistent slow-flow or persistent no reflow
  • Subject unable to tolerate anticoagulation/antiplatelet therapy per guidelines
  • Subject is enrolled in any study of an investigational device or drug that may interfere with study results

Other illness

  • Subjects with known mental or physical illness or known history of substance abuse that may cause non-compliance with the protocol, confound the data interpretation, or is associated with a life expectancy of less than one year

Other

  • Subjects presenting with cardiogenic shock at the time of the index procedure

Who the study is looking for

  • The subject is a non-pregnant female ≥18 years of age
  • The subject meets indications for PCI and stent
  • The subject is scheduled to undergo PCI with coronary IVL and stenting per standard of care for non-stented lesion
  • The subject is willing to comply with protocol-specified follow-up evaluations
  • The subject, or legally authorized representative, has been informed of the nature of the study, agrees to its provisions, and has provided written informed consent, approved by the appropriate Institutional Review Board (IRB) or Ethics Committee (EC)

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (49)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Heart and Lung Center Leipzig
Coordinator of this site? Confirm its status
LeipzigGermanyUnknown status
Universitaetsmedizin der Johannes Gutenberg - Universitaet Mainz
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MainzGermanyUnknown status
Krankenhaus der Barmherzigen Brüder Trier
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TrierGermanyUnknown status
Hospital del Mar
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BarcelonaSpainUnknown status
Hospital Universitario Reina Sofia
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CórdobaSpainUnknown status
Hospital Clínico San Carlos
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MadridSpainUnknown status
Hospital Clínico de Santiago
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Santiago de CompostelaSpainUnknown status
Centre Hospitalier d'Antibes
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AntibesFranceUnknown status
Institut Cardiovasculaire Paris Sud Hôpital Privé Jacques Cartier
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MassyFranceUnknown status
AP-HP Hopital Pitie-Salpetriere
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ParisFranceUnknown status
Clinique Pasteur
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ToulouseFranceUnknown status
Golden Jubilee National Hospital
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ClydebankUnited KingdomUnknown status
Liverpool Heart and Chest Hospital
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LiverpoolUnited KingdomUnknown status
St. George's Hospital
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LondonUnited KingdomUnknown status
Hammersmith Hospital
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LondonUnited KingdomUnknown status
Northside Hospital
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AtlantaUnited StatesUnknown status
Piedmont Heart Institute
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AtlantaUnited StatesUnknown status
Emory Hospital
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AtlantaUnited StatesUnknown status
Overlake Medical Center
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BellevueUnited StatesUnknown status
Massachusetts General Hospital
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BostonUnited StatesUnknown status
Brigham and Women's Hospital
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BostonUnited StatesUnknown status
NYU Langone Health
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BrooklynUnited StatesUnknown status
MUSC Health University Medical Center
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CharlestonUnited StatesUnknown status
The Lindner Center for Research and Education at The Christ Hospital CRA: Timothy
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CincinnatiUnited StatesUnknown status
Morton Plant Hospital
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ClearwaterUnited StatesUnknown status
Northwestern University
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EvanstonUnited StatesUnknown status
Inova Fairfax Medical Campus
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Falls ChurchUnited StatesUnknown status
University of Kansas Medical Center
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Kansas CityUnited StatesUnknown status
South Denver Cardiology Associates, P.C.
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LittletonUnited StatesUnknown status
Loma Linda University Health
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Loma LindaUnited StatesUnknown status
Good Samaritan Hospital
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Los AngelesUnited StatesUnknown status
New England Heart and Vascular Institute
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ManchesterUnited StatesUnknown status
DHR Health Heart Institute
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McAllenUnited StatesUnknown status
Vanderbilt University Medical Center
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NashvilleUnited StatesUnknown status
Centennial Heart
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NashvilleUnited StatesUnknown status
Yale New Haven Hospital
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New HavenUnited StatesUnknown status
Tulane University Center for Clinical Research
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New OrleansUnited StatesUnknown status
Columbia University Medical Center
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New YorkUnited StatesUnknown status
NYU Langone Health
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New YorkUnited StatesUnknown status
Baylor Scott & White Research Institute
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PlanoUnited StatesUnknown status
Rhode Island Hospital
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ProvidenceUnited StatesUnknown status
St. Francis Hospital
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RoslynUnited StatesUnknown status
University of Texas Health Science Center at San Antonio
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San AntonioUnited StatesUnknown status
Kaiser Permanente San Francisco Medical Center
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San FranciscoUnited StatesUnknown status
University of Washington Medical Center
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SeattleUnited StatesUnknown status
Stanford University
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StanfordUnited StatesUnknown status
Tallahassee Research Institute
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TallahasseeUnited StatesUnknown status
Montefiore Medical Center
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The BronxUnited StatesUnknown status
Wellspan York Hospital
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YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.