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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01638130
Other study ID # B322201110320
Secondary ID
Status Recruiting
Phase N/A
First received July 6, 2012
Last updated July 11, 2012
Start date February 2011

Study information

Verified date July 2012
Source Universitaire Ziekenhuizen Leuven
Contact Wendy Sterckx
Email wendy.sterckx@uzleuven.be
Is FDA regulated No
Health authority Belgium: Federal Agency for Medicinal Products and Health Products
Study type Observational

Clinical Trial Summary

The purpose of this study is to explore the experiences and needs of patients with a high-grade glioma and their caregivers. Semi-structured interviews with patients and caregivers will be conducted and analysed using Grounded-Theory approach.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adults

- Patients with a primary high-grade glioma who are treated with chemo or were treated with chemo

- Caregivers of patients with a primary high-grade glioma who are treated with chemo or were treated with chemo

- Able to be interviewed

- Dutch

Exclusion Criteria:

- Patients with cerebral metastases

- Patients and caregivers who withdraw their informed consent

- Emotionally and cognitive not being able to be interviewed

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium UZ Leuven Leuven Vlaams-Brabant

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

See also
  Status Clinical Trial Phase
Active, not recruiting NCT00308165 - Safety Study of Intracerebral Topotecan for Recurrent Brain Tumors Phase 1/Phase 2