The aim of the study is to describe pain and discomfort of an 1 hour protocol of Radial band with Statseal and a retrospective of the standard 2 hour protocol of Radial band, for the duration of the radial band and at the out-patient control.
ID
Bron
Verkorte titel
Aandoening
radial band, statseal, closure device, radialis band,
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Occlusion: will be measured using a mobile Doppler ultrasound device. This will be done after removing the R band and when the patient is visiting the out-patient department. <br>
Discomfort: will be described and measured on a scale from 1 to 5 at arrival on the CCU/CL after CAG/PCI, after removing the R band and during the first out-patient control.
Doel van het onderzoek
The aim of the study is to describe pain and discomfort of an 1 hour protocol of Radial band with Statseal and a retrospective of the standard 2 hour protocol of Radial band, for the duration of the radial band and at the out-patient control.
Onderzoeksopzet
Occlusion, Discomfort, Pain with Visual Analogue Scale : within 24 hours after CAG/PCI and within 8 weeks
Bleeding complication: 8 weeks
Use of number of different coagulantia: 8 weeks
Costs used material for radial artery compression: 8 weeks
Costs complication treatment: 8 weeks
Onderzoeksproduct en/of interventie
The research tretament concerns the duration of R band with Statseal after a coronary angiography and/or percutaneous coronary intervention, the 2 hour protocol of R band is the standard protocol and the 1 hour protocol of R band with StatSeal the experimental group in our medical center.
Publiek
H. de Lange-van Bruggen
Els Borst-Eilersplein 275
Den Haag 2545 AA
The Netherlands
0702102480
H.Lange-vanBruggen@hagaziekenhuis.nl
Wetenschappelijk
H. de Lange-van Bruggen
Els Borst-Eilersplein 275
Den Haag 2545 AA
The Netherlands
0702102480
H.Lange-vanBruggen@hagaziekenhuis.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- the subject has to be 18 years or older.
- the subject has given written informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- the subeject uses the following medication: rehopro IV during the CAG/PCI and bivalirudin.
- The coronary angiography or percutaneous coronary intervention is not being performed through the radial artery.
- The subject has a AV shunt for kidney dialysis or is a candidate for dialysis
- The subject has a known pathology that impedes the passage of arteries of the upper extremity or subclavia.
- The subeject is incompetent.
Opzet
Deelname
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL7118 |
| NTR-old | NTR7323 |
| CCMO | NL65691.098.18 |
| OMON | NL-OMON45984 |