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A Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurations (PropR)

27 lutego 2012 zaktualizowane przez: Saint Francis Care

Prospective Study Comparing the Sensed R Wave in Bipolar and Extended Bipolar Configurations

The PropR study will evaluate sensing during ventricular fibrillation (VF) in both bipolar and extended bipolar configurations, in order to evaluate if both can be used interchangeably in caring for patients. In addition, follow up evaluation of R wave amplitude over time would allow us to determine whether one configuration is more likely to be associated with change. This understanding would be important in selecting the proper configuration at the time of implant.

Przegląd badań

Szczegółowy opis

Hypothesis:

Sensing in bipolar and extended bipolar configurations are the same. However, sensing in bipolar over time is more likely to decrease when compared to extended bipolar.

Objectives:

  1. To compare bipolar sensing and extended bipolar sensing in VF.
  2. Compare sensing in bipolar and extended bipolar over time.

Methods:

  1. This study will be a randomized comparison of bipolar and extended bipolar sensing. As per usual standard of care, at the end of ICD implantation two sensing tests in VF will be performed. Patients will be randomized to sensing in VF through the device. Each patient will undergo testing in one randomized configuration followed by a second test in the other configuration. After testing at the time of implant, each patient will be seen at one month in follow up. Sensing of each configuration will be reevaluated at that time in sinus rhythm.
  2. Each patient will serve as their own control, as data for sensing in both configurations will be obtained in VF at the time of implant. During testing both signals types will be recorded simultaneously through the ICD. The primary endpoint will be duration of sensing (time to detection) in VF at the time of implant.
  3. The secondary endpoint will be sensing in sinus rhythm at one month.
  4. The patient population will include approximately 30-50 volunteers age >18, male and female, both ischemic and nonischemic cardiomyopathy, with primary and secondary implant indications.
  5. Patients will be recruited when being evaluated for defibrillator implant.
  6. Inclusion criteria: age >18 with ability to give informed consent, who are expected to live more than one year, with indication for defibrillator implant and who are not pacemaker dependent. Patients will have either ischemic or nonischemic cardiomyopathy.
  7. Exclusion criteria: age <18, inability to give informed consent, or life expectancy less than one year, pacemaker dependence, or use of preexisting lead for sensing, any condition which would preclude ICD testing at the end of the implant. Patients who are undergoing upgrade to an ICD from a pacemaker will also be excluded. In addition, patients with inherited arrhythmias or ion channel related arrhythmias will be excluded from the study.
  8. Withdrawal criteria: inability to implant device, implant lead at the RV apex, or make follow up appointment (living out of state), patient death at time of implant, elevated DFT (<10 J margin between DFT and maximum output of the device) requiring additional procedures, subcutaneous array etc.
  9. Duration of patient participation would be one month.
  10. Duration of study would be one year.

Procedures:

  1. Procedures to be followed would include screening of all eligible patients undergoing implant of a Medtronic defibrillator for either primary or secondary prevention. If patients meet inclusion criteria they would then undergo informed consent and if willing be enrolled in the study. Defibrillator implant and testing would be performed as per usual practice of the implanting physician. The RV lead will be placed at the RV apex as is usual for regular implantation of devices. However, if a lead is placed elsewhere, the patient will need to be withdrawn from the study.
  2. When VF induction is performed, sensing configuration would be tested in a randomized fashion, unblinded to the operator. The untested configuration would then be tested during second VF induction. Both tests would be performed at a sensitivity setting of 1.2mV, with a number of intervals to detection (NID) of 24/32. Final programming polarity will be left at the initially tested polarity (first DFT test), unless the operator sees a need to program differently for patient safety reasons.
  3. Medtronic defibrillators with both sensing configurations available will be used. Data collection will be performed by Dr. Tolat, Dr. Berns, Dr. Lippman, Dr. Dell'Orfano, and the study coordinator involved with the study. A data collection form and spreadsheet will be kept for use when collecting data for analysis. Follow up will be performed at one month post implant in the office.

Risk Analysis:

  1. Anticipated risks are no more than that anticipated with usual ICD implant. To date, usual implant includes induction of VF with analysis of sensing in VF and evaluation of defibrillation threshold by delivery of shock.
  2. There is no expected increased exposure to risk by performing this study.
  3. Potential benefits would include gathering additional information on sensing in VF in both configurations instead of performing the two sensing tests in one configuration. This may directly benefit the patient by allowing for reprogramming defibrillator without bringing the patient back to the hospital for further testing.

Data Analysis:

  1. Data collection will include patient information kept in a database with name kept confidential. Patients will only be identified by number in keeping with privacy laws and practice. In addition to usual patient characteristics, data variables to be collected in both configurations will include: R wave amplitude in sinus rhythm, time to detection in VF, total episode duration (time to Vfib detection and charge delivered), number of "drop outs" (undersensing) in VF, and follow up R wave amplitude in one month.
  2. Statistical Methods will compare bipolar sensing configuration to the extended bipolar configuration at baseline, sensing in VF (as measured by "drop out", time to detection), and follow up amplitude of the R wave at one month.
  3. The current expected sample size with this pilot study is 30 patients. This may require reevaluation depending on results at the time of interim analysis.

Typ studiów

Obserwacyjny

Zapisy (Rzeczywisty)

50

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

    • Connecticut
      • Hartford, Connecticut, Stany Zjednoczone, 06105
        • St Francis Hospital and Medical Center

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat i starsze (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

The patient population will include approximately 30-50 volunteers age >18, male and female, both ischemic and nonischemic cardiomyopathy, with primary and secondary implant indications.

Opis

Inclusion Criteria:

  • age > 18 with ability to give informed consent,
  • patients who are expected to live more than one year,
  • patients with indication for defibrillator implant,
  • patients who are not pacemaker dependent,
  • patients with either ischemic or nonischemic cardiomyopathy.

Exclusion Criteria:

  • age < 18,
  • inability to give informed consent,
  • life expectancy less than one year,
  • pacemaker dependence, or use of preexisting lead for sensing,
  • any condition which would preclude ICD testing at the end of the implant,
  • patients who are undergoing upgrade to an ICD from a pacemaker will also be excluded,
  • patients with inherited arrhythmias or ion channel related arrhythmias will be excluded from the study.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / Kohorta
cardiomyopathy, with implant indications
30-50 volunteers age >18, male and female with ability to give informed consent, who are expected to live more than one year, with indication for defibrillator implant and who are not pacemaker dependent.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Ramy czasowe
Duration of sensing (time to detection) in VF at the time of implant.
Ramy czasowe: At implant
At implant

Miary wyników drugorzędnych

Miara wyniku
Ramy czasowe
Sensing in sinus rhythm at one month
Ramy czasowe: One month post implant
One month post implant

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Współpracownicy

Śledczy

  • Główny śledczy: Aneesh Tolat, MD, Attending Cardiac Electrophysiologist, St Francis Hospital and Medical Center

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 grudnia 2009

Zakończenie podstawowe (Rzeczywisty)

1 lipca 2011

Ukończenie studiów (Rzeczywisty)

1 lipca 2011

Daty rejestracji na studia

Pierwszy przesłany

14 grudnia 2009

Pierwszy przesłany, który spełnia kryteria kontroli jakości

14 grudnia 2009

Pierwszy wysłany (Oszacować)

15 grudnia 2009

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Oszacować)

28 lutego 2012

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

27 lutego 2012

Ostatnia weryfikacja

1 lutego 2012

Więcej informacji

Terminy związane z tym badaniem

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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