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Nadroparine tijdens nachtelijke hemodialyse

Nadroparine tijdens de nacht

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24636
Enrollment
14
Registered
2013-09-24
Start date
2013-10-01
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

accumulation of Nadroparine during hemodialysis

Interventions

The use of 4 bloodsamples taken from the dialysisline to determine anti-Xa activity (IU/ml)

Sponsors

Stichting wetenschap Internegeneeskunde & MDL, Medisch Centrum Leeuwarden.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients (18<years of age) ondergoing nocturnal hemodialysis

Exclusion criteria

Exclusion criteria: - The use of other drugs wich block factor-Xa other than nadroparine. This includes dabigatran, apixaban, rivaroxaban, LMWH’s, heparine and fondaparinux. - The use of Cofact or Beriplex during measurements - Alteration in the dosage regime of anticoagulantia

Design outcomes

Primary

MeasureTime frame
Anti-Xa activity (IU/ml) before and after the first and last dialysis of the week to determine if accumulation occurs.

Secondary

MeasureTime frame
-Bloodflow during dialysis -Flow of dialysis fluids -Renal function -Kt-V -Bleeding events -Clotting in the dialysis filter

Contacts

Public ContactM.H. Hemmelder

H. Dunantweg 2

m.h.hemmelder@znb.nl058-2866556

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)