The aim of this study is to analyse whether or not it is possible to created a fast, reliable intraosseous entrance using the BIG and/or FAST bone needles, with less complications compared with the traditional bone needle Jamshidi.
ID
Bron
Verkorte titel
Aandoening
severely injured patients
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Primary endpoint: aspiration of bone marrow upon succesfull placement of a bone needle.
Primary parameter is: time required for successful placement.
Achtergrond van het onderzoek
Both in emergency departments and in prehospital services effort is being done to find a fast entrance to the circulation. If an intravenous access is not possible or it takes too long, intraosseous infusion is a good alternative both in adults and children. In the last few years, a few new intraosseous needles had been developed. The aim of this study is to analyze the time required to obtain a successful intraosseous entrance using the Bone Injection-Gun, Jamshidi and/or FAST1 intraosseous needles. The inserted needles will be compared on time to successful placement, adverse events and complications. The data achieved will enable us to pinpoint the best of intraosseous devices that will subsequently replace the currently used screw-tipped bone needle.
Doel van het onderzoek
The aim of this study is to analyse whether or not it is possible to created a fast, reliable intraosseous entrance using the BIG and/or FAST bone needles, with less complications compared with the traditional bone needle Jamshidi.
Onderzoeksproduct en/of interventie
The intervention consists of the application of a randomized instraosseous needle.
1. In people = > 14 years: BIG vs FAST vs conventional bone needle;
2. In children 1> and < 14 jaar: BIG vs conventional bone needle.
Publiek
P.O. Box 2040
I.B. Schipper
Rotterdam 3000 CA
The Netherlands
+31 (0)10 4635034
i.schipper@erasmusmc.nl
Wetenschappelijk
P.O. Box 2040
I.B. Schipper
Rotterdam 3000 CA
The Netherlands
+31 (0)10 4635034
i.schipper@erasmusmc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Patients in acute life threatening situations, requiring assistance of a mobile medical team;
2. Intravasculair medical or fluid resuscitation is necessary and intravasculair access cannot be obtained after two attempts.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Childeren under the age of 1 year;
2. Patients with suspected sternumanomaly (only FAST1).
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 | NL722 |
| NTR-old | NTR732 |
| Ander register | : N/A |
| ISRCTN | ISRCTN85744812 |
Samenvatting resultaten
IB. Intraosseous devices: a randomized controlled trial comparing three
intraosseous devices. Prehosp Emerg Care 2010;14(1)6-13.