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Meten van de geactiveerde stollingstijd tijdens slagaderlijke vaatingrepen.

Measuring the ACT during Non-Cardiac arterial procedures.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON29650
Enrollment
500
Registered
2018-01-21
Start date
2016-12-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

ACT

Interventions

To evaluate if the current practice of using a standardized bolus of 5000 IU of heparin during NCVI causes adequate periprocedural anticoagulation in the individual patient. This evaluation will be pe

Sponsors

dr. Arno M. Wiersema, Westfriesgasthuis.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients undergoing open or endovascular arterial non-cardiac arterial surgery aged more than 18 years.

Exclusion criteria

Exclusion criteria: All patients undergoing open or endovascular arterial non-cardiac arterial surgery aged younger than 18 years. Dialysis dependend or EGFR < 30 ml/min.

Design outcomes

Primary

MeasureTime frame
Percentage of patients reaching an ACT of 250 seconds by administering a standardized bolus of 5000 IU. Total dose of heparin needed to reach 250 seconds.

Secondary

MeasureTime frame
evaluation of predictive value of HMS to reach ACT of 250 seconds by predicted dose of heparin. All (anti)coagulation related events.

Contacts

Public ContactArno M. Wiersema
arno@wiersema.nu0229-208206

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)