Skip to content

TENS-Study - Thrombelastometry in Neurosurgical patients

TENS-Study - Thrombelastometry in Neurosurgical patients - TENS

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00034388
Enrollment
350
Registered
2024-10-09
Start date
2024-12-19
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Other pathologies with a minimum operation time of 4 hours C70 C71 C72

Interventions

Group 1: The study will include neurosurgical patients with a minimum age of 18 years who are capable of giving informed consent, who are undergoing planned surgical treatment for an underlying tumor

Sponsors

Klinik für Anästhesiologie und Operativem Intensivmedizin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Neurosurgical patients scheduled for surgery for underlying tumor - and / or minimum operation time of 4 hours - Minimum age 18 years - Signed informed consent form by patient or legally authorized person

Exclusion criteria

Exclusion criteria: refusal to participate

Design outcomes

Primary

MeasureTime frame
Primary endpoint is the correlation of lysis time with thrombembolic events in neurosurgical patients.

Secondary

MeasureTime frame
Other individual parameters of thrombelastometry, standard tests, von Willebrand factor, PAI antigen, other clinical symptoms, types of treatment and the course of the disease.

Countries

Germany

Contacts

Public ContactTobias Kammerer

Klinik für Anästhesiologie und Operative Intensivmedizin

tobias.kammerer@uk-koeln.de+49 221 478 40801

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026