The Elective PCI in Outpatient Study (EPOS) is designed to evaluate the safety and feasibility of discharge the same day as PCI, by testing the hypothesis that patients requiring extended observation can be selected effectively and that same-day…
ID
Bron
Verkorte titel
Aandoening
Stable angina.
Ondersteuning
Meibergdreef 15
1105 AZ Amsterdam
Netherlands
tel: 31 20 5669111
P.O. box 320
1110 AH Diemen
Netherlands
www.cvz.nl
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary endpoint of the study is the composite of major adverse cardiac events and severe complications of the arterial puncture with the need of blood transfusion or repeat compression, from randomization until 24 hours after PCI.
Achtergrond van het onderzoek
N/A
Doel van het onderzoek
The Elective PCI in Outpatient Study (EPOS) is designed to evaluate the safety and feasibility of discharge the same day as PCI, by testing the hypothesis that patients requiring extended observation can be selected effectively and that same-day discharge does not increase the complication rate as compared to overnight hospital stay.
Onderzoeksopzet
N/A
Onderzoeksproduct en/of interventie
After percutaneous coronary intervention, patients are observed for 4 hours.
Patients randomized to same-day discharge are ambulated after this period and discharged. Patients randomized to overnight stay are discharged the following day. Indications for extended hospital stay are based on pre-defined clinical and angiographic criteria.
Publiek
Department of Cardiology,
P.O. Box 22660
G.S. Heyde
Meibergdreef 9
Amsterdam 1100 DD
The Netherlands
+31 (0)20 5669111
g.s.heyde@amc.uva.nl
Wetenschappelijk
Department of Cardiology,
P.O. Box 22660
G.S. Heyde
Meibergdreef 9
Amsterdam 1100 DD
The Netherlands
+31 (0)20 5669111
g.s.heyde@amc.uva.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
All patients scheduled to undergo elective percutaneous coronary intervention in the Academic Medical Centre in Amsterdam who remain at home prior to the procedure.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Scheduled use of guiding catheters larger than 6 French (F) in diameter;
2. Elective use of glycoprotein 2b/3a receptor blockers;
3. Long term systemic anti-coagulation;
4. Residence of more than 60 minutes drive from an intervention center;
5. No adult care person available at home for first 24 hours after PCI;
6. Diagnostic coronary artery catheterization with possible ad hoc PCI.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL134 |
| NTR-old | NTR168 |
| Ander register | : N/A |
| ISRCTN | ISRCTN75891755 |