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NCT00083512Recruiting

Collection of Blood and Urine Samples in Patients Receiving Radiation Therapy for Glioblastoma Multiforme

Urinary and Serum VEGF and MMP Levels in Patients Receiving Radiation Therapy for Glioblastoma Multiforme: Prospective Determination of a Predictive Value for Recurrence

Source: ClinicalTrials.gov · Last updated 5 Nov 2026

Brief summary (registry, in English)

This study will collect blood and urine samples from patients undergoing radiation therapy for glioblastoma multiforme (a type of brain tumor) to investigate the effects of this treatment on blood cells and certain proteins. The information from this study may help scientists develop new tests to measure radiation exposure and find new ways to treat cancer with radiation, and help determine which kinds of patients or tumors respond better to radiation therapy. Two proteins of particular interest in this study and which may be involved in the recurrence of cancer are VEGF (vascular endothelial growth factor) and MMPs (matrix metalloproteinases). Patients 18 years of age and older with glioblastoma multiforme who are receiving or will receive radiation therapy as part of their medical treatment may be eligible for this study. Candidates are screened with a history and physical examination, blood tests, and magnetic resonance imaging (MRI) of the brain. Participants will have blood and urine samples collected before, during and after completion of their radiation treatment. Urine samples are collected in a cup and about 2 tablespoons of blood are withdrawn through a needle in a vein. Additional samples may be requested at different times during treatment and in the 3-year follow-up period.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
25 May 2004
Start date
22 Jun 2004
Lead sponsor
National Cancer Institute (NCI)
Diseases
Glioblastoma
NCT number
NCT00083512

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Gliadel wafer placement at the time of surgery.
  • Pregnancy because radiation has the potential for teratogenic or abortifacient effects.

Other illness

  • Patients with other cancers excluding non-melanomatous skin cancers or carcinoma in situ.

Other

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Criteria the registry did not label

  • INCLUSION CRITERIA:
    • Age greater than or equal to 18 years.
    • Histologically confirmed supratentorial Glioblastoma multiforme.
    • Karnofsky performance \>60.
    • Patient must be a candidate for radiotherapy.
    • Ability of subject or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document.

Age in the registry: 18 years to 120 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Institutes of Health Clinical Center
Coordinator of this site? Confirm its status
BethesdaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.