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INcidence of Deep vein thRombosis after Arthroplasty of the shoulder

INcidence of Deep vein thRombosis after Arthroplasty of the shoulder - INDRA-P

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31366
Enrollment
100
Registered
2007-08-02
Start date
2008-03-01
Completion date
Unknown
Last updated
2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

venous thromboembolism blood clot

Interventions

None listed

Sponsors

Isala Klinieken
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: arthroplasty shoulder Over 18 years

Exclusion criteria

Exclusion criteria: Anticoagulantia (heparin-derivates, Vit K antagonists) Follow-up not feasible no informed consent Previous trombosis

Design outcomes

Primary

MeasureTime frame
De onderzoeksperiode is 6 weken. Primaire uitkomstmaat is de incidentie van postoperatieve symptomatische en asymptomatische tromboembolische complicaties aangetoond middels uitgebreide compressie echo-duplex.

Secondary

MeasureTime frame
Secundaire uitkomstmaten zijn de incidentie van bloedingen gedefinieerd als: Een majeure bloeding peri-operatief (Hb daling > 2 mmol/l of transfusie behoefte) Een kleine bloeding (elke andere zichtbare bloeding)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)