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Recruiting NCT06709833

Meningioma and Embolism Thrombosis Risk & Investigation of Coagulation

Observational Meningeoma Thrombembolism Surgical Resection

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Meningeoma, Thrombembolism, Surgical Resection. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Germany
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Despite being generally benign tumors, meningiomas are associated with an increased risk for thrombembolic complications after surgical resection. The molecular mechanisms underlying this circumstance are still unknown. In this prospective observational trial, the investigators aim to evaluate the changes in coagulation and platelet function caused by tumor resection. Blood samples are obtained by patients undergoing meningioma resection before and immediately after resection to detect said changes. As a control cohort, blood samples are obtained from patients undergoing resection for glioma.

Primary outcome measures

  • Tissue factor [Time frame: duration of surfical tumor resection (a few hours)]

Eligibility criteria

Inclusion criteria

  • Patients undergoing resection for meningioma or
  • Patients undergoing resection for glioma or
  • Healthy controls
  • written consent for study participation

Exclusion criteria

\-

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Germany · 1 center
  • University Hospital for Anaesthesiology and Intensive Care Medicine, Tuebingen — Tübingen

Identifiers

NCT: NCT06709833 · 001_2024_BO2

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗