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WithdrawnNCT01331616Updated Dec 9, 2021

Optic Neuropathy in 10 Patients With Glioblastoma Receiving Bevacizumab

An Early Phase 1 interventional study of Bevacizumab (Avastin) in Glioblastoma and Optic Neuropathy, sponsored by West Penn Allegheny Health System. Withdrawn. Per ClinicalTrials.gov, last updated 2021-12-09.

Sponsored by West Penn Allegheny Health System · Early Phase 1, Interventional, and Treatment

Phase
Early Phase 1
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Sex
All
01

Study summary

Does treatment with bevacizumab (Avastin) in combination with prior or current radiotherapy lead to optic neuropathy?

Read the detailed description

The investigators research will focus on patients prior to them beginning treatment with bevacizumab (Avastin), by undergoing a baseline visual examination with Visual evoked Potentials testing. This will allow testing of the patient's optic nerve function bilaterally. Patients will then begin their normally scheduled treatment with avastin, and other chemotherapeutic agents, as well any radiation treatments scheduled. Once patients have completed their treatment with avastin for 6-8 weeks, they will then undergo their second Visual Evoked Potential testing, with both studies then being compared for any changes within the optic nerves. Patients will also be recommended to have stringent follow up with an Ophthalmologist to include confrontational visual field testing, external and anterior segment examination, and dilated fundus examination. The investigators main objective is to assess whether or not bevacizumab causes a direct toxic effect on patient's optic nerves leading to an acute/subacute optic neuropathy.

02

Conditions studied

  • Glioblastoma
  • Optic Neuropathy

Keywords

  • Prospective study
  • Glioblastoma
  • Avastin
  • Visual Evoked Potential
  • Optic neuropathy
  • Chemo-radiotherapy
03

In context

Glioblastoma

1,920 studies on the registry are indexed under Glioblastoma; 450 are open to participants now.

Browse Glioblastoma studies →

Lead sponsor

West Penn Allegheny Health System is the lead sponsor of 18 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosed w Glioblastoma grade IV, and scheduled to begin chemo radiotherapy with Avastin

Exclusion criteria

Exclusion Criteria:

  • No diagnosis of GBM, not scheduled to begin treatment with avastin in combination with radiotherapy.
05

Study design

Phase
Early Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Bevacizumab (Avastin)

    Drug: Bevacizumab (Avastin)

Interventions

  • DrugBevacizumab (Avastin)

    Dosage is: 10 mg/kg every 2 weeks as monotherapy or in combination (unlabeled) with irinotecan. Patients will also receive Radiotherapy prior to beginning chemotherapy.

06

What researchers measure

Primary outcomes

  1. Measurement of Visual Evoked Potentials (optic nerve function and visual processing) and optic nerve function in 10 patients.

    Does Avastin lead to optic neuropathy in combination w chemo-radiotherapy? Our research will focus on patients prior to them beginning treatment with bevacizumab (Avastin), by undergoing Visual evoked Potentials testing. This will allow testing of the patient's optic nerve function bilaterally. In our study of VEP, we will be measuring optic nerve function, to asses if there has been any damage.

    Time frame: 1 year

Secondary outcomes

  1. Number of patients diagnosed with optic neuropathy following treatment with chemo and radiation in combination with avastin treatment

    The investigators will compare the results of the patient's Visual Evoked Potential (VEP) testing performed prior to treatment with Avastin and chemo-radiotherapy to the results of the VEP after completion to assess optic nerve function; and any signs of direct optic neuropathy In our study the investigators will compare the results of the Visual Evoked Potential results performed prior to the chemoradiation to results of the Visual Evoked Potential after completion of standard-of-care treatment for glioblastoma.

    Time frame: 1 year

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 9, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01331616
Lead sponsor
West Penn Allegheny Health System
Responsible party
Dawnmarie DeFazio (Physician, West Penn Allegheny Health System) — Principal investigator
First posted
Apr 8, 2011
Start date
Mar 2011
Primary completion
Jul 2012
Completion
Jul 2012
Last update
Dec 9, 2021

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Nov 2021. You cannot join it, but the record below documents what was studied.

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