Patient-Reported Outcome Measure for Meningiomas study
- Conditions
- benign primary brain tumorMeningioma10029209
- 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
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
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
Name Time Method
- Secondary Outcome Measures
Name Time Method