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Patient-Reported Outcome Measure for Meningiomas study

Recruiting
Conditions
benign primary brain tumor
Meningioma
10029209
Registration Number
NL-OMON43114
Lead Sponsor
eids Universitair Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
165
Inclusion Criteria

In order to be eligible to participate in this study, a subject should:
1. be diagnosed clinically or histopathologically with a WHO grade 1 meningioma
2. be 18 years or older
3. give written informed consent prior to inclusion

Exclusion Criteria

A potential subject who meets any of the following criteria will be excluded from participation in this study:
1. Patients with a neurofibromatosis type 2 meningioma.
2. Patients not fluent in Dutch, English or Italian (depending on the country where they live).
3. Patients with physical or mental conditions interfering with the understanding and completion of questions and questionnaires.

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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