Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:24 PM
Ignite Modification Date:
2025-12-24 @ 7:24 PM
NCT ID:
NCT00463203
Eligibility Criteria:
Inclusion criteria:
* Written informed consent
* Histological verification of primary malignant brain tumor, or grade II glioma, meningeoma or ependymoma with progression and no other treatment options (including brain stem gliomas without histological verification)
* Recurrence or progression after standard treatment (debulking surgery of possible, radiotherapy and for grade III or IV tumors temozolomide or other chemotherapy.
* Evidence of measurable recurrent progressive disease (CT/MRI scan)
* An interval of at least 4 weeks between prior surgical resection and study enrollment
* An interval of at least 4 weeks between prior radiotherapy or chemotherapy and enrollment on this protocol.
* PS 0-2 (ECOG scale)
* Age \> 18
* Life expectancy \> 3 month
* Normal organ function:
* Platelets \> 125 x 109/l
* Hemoglobin \>6,2 mmol/l
* Leukocytes \> 3 x 109/l
* ACN\> 1,5 x 109/l
* ASAT or ALAT \< 3 x upper normal limit
* Bilirubin \< 1,5 x upper normal limit
* Creatinine clearance \> 45 ml/min
* APTT \< normal limit
* INR \< normal limit
* Fertile females must use oral contraceptive, IUD (intrauterine device), gestagen sustained release injection, subdermal implantation, transdermal patch or hormonal vaginal ring. This must continue at least three months after the patients is off-study. Fertile males must use preservatives
* No sign of cerebral bleeding
Exclusion criteria:
* Radiotherapy or chemotherapy within the last 4 weeks.
* Co-medication that may interfere with study results; e.g. immuno-suppressive agents other than corticosteroids
* Prior VEGF-based therapy
* Any condition (medical, social, psychological), which would prevent adequate information and follow-up
* Any other concurrent active malignancy, except, adequately treated basal or squamous cell carcinoma of the skin, or carcinoma in situ.
* Any significant cardiac disease (New York Heart Association Class II or greater), arrhythmia, congestive heart failure, acute myocardial infarction within 6 months or unstable angina pectoris.
* Clinically significant peripheral vascular disease
* Evidence of bleeding diathesis, coagulopathy or taking ASA, NSAIDs or clopidogrel
* Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to day 0, anticipation of need for major surgical procedure during the curse of the study
* Minor surgical procedures, fine needle aspirations or core biopsies within 7 days prior to day 0
* History of abdominal fistula, gastrointestinal perforation or intra-abdominal abscess within 6 month prior to day 0
* History of known HIV, Hepatitis B and Hepatitis C negative
* Any ongoing infection, uncontrolled diabetes mellitus, serious non-healing wound, ulcer or bone fracture
* Pregnancy or breast feeding
* Requires therapeutic anti-coagulation
* Blood pressure \> 150/100 mmHG
* Grade 2 or greater proteinuria
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00463203
Study Brief:
Protocol Section:
NCT00463203