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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00019578
Other study ID # 990011
Secondary ID 99-C-0011CDR0000
Status Completed
Phase Phase 1
First received
Last updated
Start date November 1998
Est. completion date May 2002

Study information

Verified date March 2012
Source National Institutes of Health Clinical Center (CC)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. PURPOSE: Phase I trial to study the effectiveness of stereotactic radiosurgery in treating patients who have brain tumors.


Description:

OBJECTIVES: I. Establish stereotaxic radiosurgery as a treatment technique at the National Institute of Health in patients with intracranial neoplasms. II. Assess the response rate, local control, time to progression, pattern of failure, and magnetic resonance spectrographic data following this therapy in these patients. PROTOCOL OUTLINE: All patients undergo stereotaxic head frame placement, followed by stereotaxic radiosurgery on day 1. The dosage of radiation therapy administered is dependent on the tumor diameter. Patients are followed at 2 and 6 weeks and then every 3 months for 5 years. PROJECTED ACCRUAL: Up to 30 patients will be accrued for this study within 7-10 months.


Other known NCT identifiers
  • NCT00001791

Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date May 2002
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Histologically proven intracranial tumor OR Pathologically confirmed cancer with metastases to the brain OR Newly discovered brain lesions that are amenable to stereotaxic biopsy No more than 3 measurable tumors Only 1 tumor more than 3 cm in diameter that requires radiosurgery allowed No tumor more than 4 cm in diameter No tumor that involves more than 50% of the brain stem --Prior/Concurrent Therapy-- Biologic therapy: Not specified Chemotherapy: Not specified Endocrine therapy: Concurrent corticosteroids allowed Radiotherapy: Prior cranial radiotherapy allowed Surgery: Radiosurgery to other nonstudy intracranial lesions allowed Prior biopsy and/or subtotal or near-total resection allowed --Patient Characteristics-- Age: 18 and over Performance status: Karnofsky 70-100% OR ECOG 0-2 Life expectancy: More than 3 months Hematopoietic: WBC at least 3,000/mm3 Absolute granulocyte count at least 500/mm3 Hemoglobin at least 10 g/dL Platelet count at least 50,000/mm3 Hepatic: SGOT or SGPT no greater than 2.5 times upper limit of normal (ULN) PT and PTT no greater than 1.5 times ULN No clinically significant hepatic dysfunction Renal: Creatinine no greater than 1.3 times ULN Cardiovascular: No clinically significant cardiac dysfunction Pulmonary: No clinically significant pulmonary dysfunction Other: Not pregnant or nursing Negative pregnancy test No clinically significant systemic illness or serious infection that would preclude study compliance No other organ dysfunction that would preclude study compliance No history of psychiatric disease No allergy to contrast agent Papilledema and motor or sensory deficits allowed No contraindications to MRI (e.g., aneurysm clip, implanted neural stimulator, implanted cardiac defibrillator, cochlear implant, ocular foreign body or implant, or insulin pump)

Study Design


Related Conditions & MeSH terms

  • Adult Brain Stem Glioma
  • Adult Central Nervous System Germ Cell Tumor
  • Adult Craniopharyngioma
  • Adult Ependymoma
  • Adult Infiltrating Astrocytoma
  • Adult Malignant Meningioma
  • Adult Medulloblastoma
  • Adult Meningioma
  • Adult Noninfiltrating Astrocytoma
  • Adult Oligodendroglioma
  • Adult Pineal Parenchymal Tumor
  • Astrocytoma
  • Brain Metastases
  • Brain Neoplasms
  • Craniopharyngioma
  • Ependymoma
  • Glioma
  • Medulloblastoma
  • Meningioma
  • Mixed Gliomas
  • Neoplasm Metastasis
  • Neoplasms
  • Neoplasms, Germ Cell and Embryonal
  • Neuroectodermal Tumors
  • Neuroectodermal Tumors, Primitive
  • Neuroectodermal Tumors, Primitive, Peripheral
  • Oligodendroglioma
  • Pinealoma
  • Sarcoma, Ewing
  • Stage IV Peripheral Primitive Neuroectodermal Tumor

Intervention

Procedure:
Sterotactic radiosurgery


Locations

Country Name City State
United States Radiation Oncology Branch Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Institutes of Health Clinical Center (CC)

Country where clinical trial is conducted

United States, 

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