Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Intervention (ABCD-PCI)
26. července 2011 aktualizováno: Icahn School of Medicine at Mount Sinai
Ambulatory Closure Device Percutaneous Intervention: a Multi-Center Randomized Trial Evaluating Patient Satisfaction, Safety, and Cost Effectiveness of Ambulatory PCI in the Current Era
This is a multi-center trial that will evaluate the safety, feasibility, and cost effectiveness of discharging patients, who have had successful percutaneous coronary intervention (PCI) and deployment of the AngiomaxTM closure device, 6 hours after against 24 hours after the procedure.
Patients will be randomized in a 3 (test): 1 (control) fashion and will have a study population of 600 patients over 6 investigational sites all within the United States.
Patients <65 years old will be chosen in order to stay within the low risk group and will be followed up after 24 hours, 7 days, and 30 days via phone or office visit.
The primary endpoint will be a composite of major adverse cardiac and cerebral events, and the incidence of major bleeding or vascular complications.
Data acquired from the study, such as blinded financial information and patient satisfaction surveys, will be used in order to evaluate cost analysis and safety of the procedure.
Přehled studie
Postavení
Dokončeno
Podmínky
Intervence / Léčba
Detailní popis
Closure devices are a relatively new method for sealing the femoral arterial puncture following procedures including percutaneous intervention (PCI).
Because the risk of severe complications (e.g., bleeding, myocardial infarction, stroke, and mortality) associated with PCI when closure devices are very low, many patients undergoing PCI may be considered eligible for a same day hospital discharge.
As the practice of ambulatory PCI is becoming more common, it is important to evaluate the readiness of patients under-going PCI for same-day discharge and anxiety and coping abilities of patients post-discharge.
Our hypothesis is that same day discharge of patients who have undergone a PCI procedure with closure using a vascular closure device is safe, patients will be comfortable with a same day discharge and this process will be more cost efficient than the current standard of staying in the hospital overnight.
The current pilot study is a multi-center, randomized parallel arm, controlled trial of low-risk patients undergoing an elective PCI procedure.
Overall, 600 patients will be enrolled.
After providing informed consent, participants will be randomized to leave the hospital on the same day as the PCI procedure or stay overnight in a 1:1 ratio.
Data collection includes a self-administered questionnaire at hospital discharge, telephone interviews at 7-days and 30-days post-hospital discharge, and chart abstraction.
The primary outcome for this study is differences across randomization arm in patient satisfaction scores on the validated 10-item Post-discharge coping difficulty scale assessed 7 days post-discharge.
Secondary outcomes will include differences across randomization group for symptoms of anxiety, readiness for hospital discharge, patient satisfaction with the timing of their discharge, post-procedure pain and soreness, and cost-savings.
While a data safety monitoring board will track all adverse events (i.e., myocardial infarction, hematoma, hospitalizations, and mortality), we anticipate too few events to occur to make meaningful inferences beyond that PCI is safe regardless of the timing of hospital discharge.
The data from this pilot study will determine the comfort patients experience after undergoing PCI with an ambulatory (i.e, same-day) hospital discharge.
Furthermore, this pilot study will provide the foundation for a large scale non-inferiority study of same-day discharge on outcomes including myocardial infarction, bleeding, and mortality.
Such data will indicate the overall feasibility of early ambulatory PCI and has the potential to radically alter health care delivery following PCI.
Typ studie
Pozorovací
Zápis (Aktuální)
303
Kontakty a umístění
Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.
Studijní místa
-
-
New York
-
New York, New York, Spojené státy, 10029
- Mount Sinai School of Medicine
-
-
Texas
-
Dallas, Texas, Spojené státy, 75226
- Baylor University Medical Center
-
-
Kritéria účasti
Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.
Kritéria způsobilosti
Věk způsobilý ke studiu
18 let až 75 let (Dospělý, Starší dospělý)
Přijímá zdravé dobrovolníky
Ne
Pohlaví způsobilá ke studiu
Všechno
Metoda odběru vzorků
Ukázka pravděpodobnosti
Studijní populace
The target population for this study will include patients undergoing an elective PCI.
Overall, 600 patient will be recurited from two sites in the United Sates.
As this is a feasiblity study, enrollment will be restricted to low-risk patients.
For this reason, the study will be limited to patients under 75 years of age.
All patients must meet all of the inclusion criteria and have none of the exclusion criteria to be enrolled into the study.
Popis
Inclusion Criteria:
. <75 years of age at the time of procedure.
2. Patient has a type A or B lesion(s)
3. Femoral access site is amenable to closure with a vascular closure device.
4. Over 2 hours since the completion of the PCI procedure (at least 2 hours must elapse from completion of the PCI before subjects become eligible).
Exclusion Criteria:
- Patient has a life expectancy less than 12 months.
- Patient has recent evidence of an acute coronary syndrome (MI)
- Femoral access is difficult or site is not amenable to closure device
- Anticoagulants other than unfractionated heparin or bivalirudin were used during the procedure (i.e. enoxaparin).
- Patient has sub optimal angiographic outcome or clinical complication(s) during PCI
- The PCI occurred in something other than a native coronary artery
- Angiographic evidence of thrombus
- Patient has more than 3 stents implanted during this PCI
- Patient has an INR >2, Platelet count <100,000 or Hematocrit <25
- Occlusion of major side branch during PCI of >1.5mm
- Patient has ejection fraction ≤30%
- Known allergy to PCI procedural medications
- Patient reports living further than 30 minutes from a hospital by ambulance.
- Patient provides informed consent and agrees to the follow-up schedule.
- Evidence of vascular complication(s) (e.g. dissection, hematoma, bleeding) peri-procedure
- Patient is pregnant
- Evidence of infection (e.g. fever, pus, swelling) peri-procedure
- Patients with chronic renal insufficiency (e.g. serum creatinine ≥1.5 mg/dL)
Studijní plán
Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.
Jak je studie koncipována?
Detaily designu
- Observační modely: Case-Control
- Časové perspektivy: Budoucí
Kohorty a intervence
Skupina / kohorta |
Intervence / Léčba |
|---|---|
|
overnight
Subjects that stay overnight at the hospital.
|
At six hours post-PCI,patients will be randomized to be discharged immediately or to stay overnight in the hospital for observation and discharged the following day.
Randomization will occur in a 1:1 ratio.
Additionally, randomization will be performed stratified by study site.
|
|
Next Day Discharge
Subjects that are discharged on the same day of the procedure.
|
At six hours post-PCI,patients will be randomized to be discharged immediately or to stay overnight in the hospital for observation and discharged the following day.
Randomization will occur in a 1:1 ratio.
Additionally, randomization will be performed stratified by study site.
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Post-hospitalization patient satisfaction
Časové okno: 30 days after enrollment
|
The primary endpoint is the difference in post-hospitalization patient satisfaction during the initial seven days following PCI.
Post-hospitalization patient satisfaction will be assessed using the 10-item Post-Discharge Coping Difficulty scale.
|
30 days after enrollment
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Patient satisfaction with timing of discharge
Časové okno: 30 days after enrollment
|
Secondary outcomes will include post-hospital anxiety, readiness for hospital discharge, patient satisfaction with the timing of their discharge, post-procedure pain and soreness, resource utilization and cost-savings.
|
30 days after enrollment
|
|
Patient Satisfaction Outcome Assessment
Časové okno: 30 days After Enrollment
|
These outcomes will be assessed using standardized questionnaires and validated techniques.
The composite of major adverse cardiac events (MACE) and cerebral events and the incidence of major bleeding or vascular complications will be monitored for all patients through the 30 day follow-up period.
|
30 days After Enrollment
|
Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Spolupracovníci
Vyšetřovatelé
- Vrchní vyšetřovatel: Michael C Kim, MD, Icahn School of Medicine at Mount Sinai
Publikace a užitečné odkazy
Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.
Termíny studijních záznamů
Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.
Hlavní termíny studia
Začátek studia
1. ledna 2008
Primární dokončení (Aktuální)
1. června 2010
Dokončení studie (Aktuální)
1. června 2010
Termíny zápisu do studia
První předloženo
31. března 2010
První předloženo, které splnilo kritéria kontroly kvality
27. října 2010
První zveřejněno (Odhad)
29. října 2010
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
28. července 2011
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
26. července 2011
Naposledy ověřeno
1. července 2011
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- GCO 07-1324
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .