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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00392548
Other study ID # RTOG0611
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 25, 2006
Last updated October 25, 2006
Start date October 2006
Est. completion date October 2006

Study information

Verified date September 2006
Source Tel-Aviv Sourasky Medical Center
Contact Deborah T Blumenthal, MD
Phone 011972524266304
Email deborahblumenthal@gmail.com
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Study of the urinary vascular endothelial growth factor (VEGF) levels in patients with glioblastoma, receiving standard therapy.

Hypothesis: that urinary VEGF levels can serve as a predictor of treatment response and survival.


Description:

Measurement of urinary VEGF levels pre treatment,immediately after treatment, and 1 month after treatment


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 130
Est. completion date October 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient must be enrolled on an RTOG GBM study that prescribes 6000 cGy of radiation therapy.

- Patient must meet the eligibility requirements for the RTOG treatment study. (If the patient is deemed retrospectively ineligible for the RTOG treatment study, the patient will likewise be ineligible for this study.)

- Patient must sign a study-specific informed consent for RTOG 0611 prior to study entry.

Exclusion Criteria:

- Patient not able to receive 6000 cGy of radiation therapy.

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Locations

Country Name City State
Israel tel Aviv Sourasky Medical Center Tel Aviv

Sponsors (2)

Lead Sponsor Collaborator
Tel-Aviv Sourasky Medical Center Radiation Therapy Oncology Group

Country where clinical trial is conducted

Israel, 

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