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Paclitaxel Releasing Balloon in Patients Presenting With In-Stent Restenosis (PEPPER)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00961181
First Posted: August 18, 2009
Last Update Posted: May 6, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Biotronik AG
August 13, 2009
August 18, 2009
March 19, 2013
May 3, 2013
May 6, 2013
August 2009
December 2010   (Final data collection date for primary outcome measure)
In-stent Late Lumen Loss [ Time Frame: 6 months ]

In-stent is defined as from proximal shoulder to distal shoulder of the dilated Pantera Lux balloon.

Late lumen loss is defined as the difference between minimal luminal diameter after procedure and at 6 months, as evaluated by offline quantitative coronary angiography (QCA).

Offline quantitative coronary angiography (QCA) analysis was performed by an independent core laboratory (Ulrich Dietz, MD, Deutsche Klinik für Diagnostik, Wiesbaden, Germany).

Late Lumen Loss (in-stent) [ Time Frame: 6 months ]
Complete list of historical versions of study NCT00961181 on ClinicalTrials.gov Archive Site
  • In-segment Late Lumen Loss [ Time Frame: 6 months ]

    In-segment is defined as from proximal shoulder to distal shoulder of the dilated Pantera Lux balloon plus 5 mm proximal and 5 mm distal.

    Late lumen loss is defined as the difference between minimal luminal diameter after procedure and at 6 months, as evaluated by offline quantitative coronary angiography (QCA).

    Offline quantitative coronary angiography (QCA) analysis was performed by an independent core laboratory (Ulrich Dietz, MD, Deutsche Klinik für Diagnostik, Wiesbaden, Germany).

  • Cumulative Major Adverse Cardiac Events Rate (Composite of Cardiac Death, Non-fatal Myocardial Infarction, Clinically Driven Target Lesion Revascularization, Clinically Driven Target Vessel Revascularization) [ Time Frame: 6 months ]

    All safety endpoint and serious adverse events were adjudicated by an independent clinical events committee.

    Major Adverse Cardiac Events = MACE Myocardial Infarction = MI Target Lesion Revascularization = TLR Target Vessel Revascularization = TVR

  • Cumulative MACE Rate (Composite of Cardiac Death, Non-fatal MI, Clinically Driven TLR, Clinically Driven TVR) [ Time Frame: 12 months ]
    All safety endpoint and serious adverse events were adjudicated by an independent clinical events committee.
  • In-stent Diameter Stenosis (%DS) [ Time Frame: 6 months ]

    In-stent is defined as from proximal shoulder to distal shoulder of the dilated Pantera Lux balloon.

    Diameter stenosis is defined as the difference between reference vessel diameter and minimal lumen diameter divided by reference vessel diameter x100%.

    Offline quantitative coronary angiography (QCA) analysis was performed by an independent core laboratory (Ulrich Dietz, MD, Deutsche Klinik für Diagnostik, Wiesbaden, Germany).

  • In-segment Diameter Stenosis (%DS) [ Time Frame: 6 months ]

    In-segment is defined as from proximal shoulder to distal shoulder of the dilated Pantera Lux balloon plus 5 mm proximal and 5 mm distal.

    Diameter stenosis is defined as the difference between reference vessel diameter and minimal lumen diameter divided by reference vessel diameter x100%.

    Offline quantitative coronary angiography (QCA) analysis was performed by an independent core laboratory (Ulrich Dietz, MD, Deutsche Klinik für Diagnostik, Wiesbaden, Germany).

  • Binary In-stent Restenosis [ Time Frame: 6 months ]

    In-sent is defined as from proximal shoulder to distal shoulder of the dilated Pantera Lux balloon.

    Binary restenosis was defined as a ≥ 50% diameter stenosis at follow-up as evaluated by offline quantitative coronary angiography (QCA).

    Diameter stenosis is defined as the difference between reference vessel diameter and minimal lumen diameter divided by reference vessel diameter x100%.

    Offline quantitative coronary angiography (QCA) analysis was performed by an independent core laboratory (Ulrich Dietz, MD, Deutsche Klinik für Diagnostik, Wiesbaden, Germany).

  • Binary In-segment Restenosis [ Time Frame: 6 months ]

    In-segment is defined as from proximal shoulder to distal shoulder of the dilated Pantera Lux balloon plus 5 mm proximal and 5 mm distal.

    Binary restenosis was defined as a ≥ 50% diameter stenosis at follow-up as evaluated by offline quantitative coronary angiography (QCA).

    Diameter stenosis is defined as the difference between reference vessel diameter and minimal lumen diameter divided by reference vessel diameter x100%.

    Offline quantitative coronary angiography (QCA) analysis was performed by an independent core laboratory (Ulrich Dietz, MD, Deutsche Klinik für Diagnostik, Wiesbaden, Germany).

  • Technical Success [ Time Frame: directly after intervention (after finalized treatment) ]

    Technical success is defined as successful vascular access, completion of the endovascular procedure and immediate morphological success with < 30% residual diameter stenosis assessed by quantitative coronary angiography (QCA).

    Diameter stenosis is defined as the difference between reference vessel diameter and minimal lumen diameter divided by reference vessel diameter x100%.

    Offline quantitative coronary angiography (QCA) analysis was performed by an independent core laboratory (Ulrich Dietz, MD, Deutsche Klinik für Diagnostik, Wiesbaden, Germany).

  • Device Success [ Time Frame: directly after intervention (after finalized treatment) ]

    Device success defined as exact deployment of the device as documented by two different projections assessed by quantitative coronary angiography (QCA).

    Offline quantitative coronary angiography (QCA) analysis was performed by an independent core laboratory (Ulrich Dietz, MD, Deutsche Klinik für Diagnostik, Wiesbaden, Germany).

  • In-segment Late Lumen Loss [ Time Frame: 6 months ]
  • Percent in-stent diameter restenosis [ Time Frame: 6 months ]
  • Percent in-segment diameter restenosis [ Time Frame: 6 months ]
  • Binary In-stent Restenosis [ Time Frame: 6 months ]
  • Binary In-segment Restenosis [ Time Frame: 6 months ]
  • Cumulative MACE rate [ Time Frame: 1, 6 and 12 months ]
  • Type of reoccurrence according to Mehran classification [ Time Frame: 6 months ]
  • Technical Success [ Time Frame: directly after intervention (after finalized treatment) ]
  • Device Success [ Time Frame: directly after intervention (after finalized treatment) ]
Not Provided
Not Provided
 
Paclitaxel Releasing Balloon in Patients Presenting With In-Stent Restenosis
Paclitaxel Releasing Balloon in Patients Presenting With In-Stent Restenosis A Prospective, Multi-centre, Non-randomized Clinical Trial With Follow-up Investigations at 1, 6 and 12 Months
The primary objective of this study is to evaluate the safety and efficacy of the paclitaxel releasing balloon in patients with in-stent restenosis in a coronary artery.

All patients are treated with the paclitaxel releasing balloon Pantera Lux. The indication is in-stent restenosis in either bare metal stent (BMS) or drug eluting stent (DES).

Clinical follow up visits at 1, 6 and 12 months. Angiographic follow up visit at 6 months.

Interventional
Not Provided
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
In-stent Coronary Artery Restenosis
Device: Paclitaxel Releasing Balloon
Percutaneous coronary intervention with paclitaxel releasing balloon
Other Name: Pantera Lux
Experimental: Paclitaxel Releasing Balloon
Percutaneous coronary intervention with paclitaxel releasing balloon
Intervention: Device: Paclitaxel Releasing Balloon
Hehrlein C, Dietz U, Kubica J, Jørgensen E, Hoffmann E, Naber C, Lesiak M, Schneider H, Wiemer M, Tölg R, Richardt G. Twelve-month results of a paclitaxel releasing balloon in patients presenting with in-stent restenosis First-in-Man (PEPPER) trial. Cardiovasc Revasc Med. 2012 Sep-Oct;13(5):260-4. doi: 10.1016/j.carrev.2012.06.002. Epub 2012 Aug 4.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
81
May 2011
December 2010   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Patient >/= 18 years
  2. Written patient informed consent available
  3. Patients with stable, unstable or documented silent angina pectoris
  4. Patient eligible for percutaneous coronary intervention
  5. Patient acceptable candidate for coronary artery bypass surgery
  6. Patients with a single restenotic lesion in a previously stented area of a coronary artery (irrelevant whether BMS or DES related)
  7. Target reference vessel diameter (visual estimation): 2 - 4 mm
  8. Target lesion length (visual estimation): 8 - 28 mm
  9. Target lesion stenosis (visual estimation): >/= 50% - < 100%

Exclusion Criteria:

  1. Left ventricular ejection fraction of < 30%
  2. Visible thrombus in the target vessel visualized by angiography
  3. Myocardial infarction (STEMI/NSTEMI) within 72 hours of the intended treatment. Determination of CKMB and/or troponin T or I is required.

    Notes:

    Laboratory assessments to be done within 24 hours prior to intervention. Patients with CKMB and/or troponin T or I > 2 fold the upper limit of normal must not be included in the trial.

  4. Patients with planned major surgery within 3 months after planned coronary intervention and/or risk of either acetylsalicylic acid of clopidogrel cessation
  5. Lesion length longer than length of available treatment balloon
  6. Impaired renal function (serum creatinine > 2.0mg/dl or 177 micro mol/l, determined within 72 hours prior to intervention)
  7. Additional coronary lesions (restenotic or de novo) in the same vessel which requires treatment
  8. Totally occluded coronary artery (Mehran classification IV and TIMI flow 0)
  9. Target lesion located in vessel bifurcation
  10. Previous and/or planned brachytherapy of target vessel
  11. Target lesion located in left main coronary artery
  12. Stroke or TIA < 6 months prior to procedure
  13. Patient with signs of a cardiogenic shock
  14. Patient under ongoing systemic immunosuppressive therapy with paclitaxel or agents of the -limus group (i.e. sirolimus, tacrolimus, everolimus)
  15. Surgeries of any kind within 30 days prior to screening
  16. Patient with bleeding diathesis in whom anticoagulation or antiplatelet medication is contraindicated
  17. Known allergies to anti-platelet-, anticoagulation therapy, contrast media or paclitaxel
  18. Pregnant and/or breast-feeding females or females who intend to become pregnant (pregnancy test required for females of child-bearing potential)
  19. Patient with a life expectancy of less than one year
  20. Patient currently enrolled in other investigational device or drug trial
  21. Patient with known incompliance to medical (antiplatelet, anticoagulation) therapy
  22. Patient not able or willing to adhere to follow-up visits including follow-up angiography
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
 
NCT00961181
C0902
Yes
Not Provided
Not Provided
Biotronik AG
Biotronik AG
Not Provided
Principal Investigator: Christoph Hehrlein, MD University Medical Center, Freiburg i.Br., Germany
Biotronik AG
May 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP