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Hemostatic function one year after orthotopic liver transplantation

Hemostatic function one year after orthotopic liver transplantation - HALT

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37729
Enrollment
82
Registered
2012-08-06
Start date
2012-09-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

coagulation hemostasis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patient group: - >18 year - Signed informed consent - First liver transplantation with a full-size graft - Adequate graft function in past year follow-up Control group of healhty volunteers: - >18 year - Signed informed consent

Exclusion criteria

Exclusion criteria: Patient group: - Documented history of congenital coagulation disorder - Active infection - Active rejection - Disease recurrence - Graft failure - Use of anticoagulant medicine within a period prior to the blood draw that is shorter than the wash-out period of the specific drug (typically within 10 days of the blood draw). - Pregnancy Control groupof healthy volunteers: - Documented history of congenital coagulation disorder - History of vascular disease - History of hepatic disease - History of any systemic disease - Recent viral infection (

Design outcomes

Primary

MeasureTime frame
Thrombin generation by Calibrated Automated Thrombinography

Secondary

MeasureTime frame
- Platelet activatability as evidenced by flow cytometry - Plasma levels of VWF and ADAMTS13 - Fibrinolytic potential as assessed by a plasma-based clot lysis assay

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)