ClinicalTrials.gg
Status unknownNCT00686387Updated Apr 12, 2011

Establishment of a Brain and Spinal Tumor Tissue Bank

An observational study in Glioblastoma Multiforme, Glioma and Neuroectodermal Tumors, sponsored by Taipei Medical University WanFang Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2011-04-12.

Sponsored by Taipei Medical University WanFang Hospital · Observational

The sponsor has not verified this record recently (last verified Apr 2011), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
70
Ages
20 Years and older
Sex
All
01

Study summary

The purpose of this study is to establish a Brain and Spinal Tumor Tissue/Specimen repository to serve as a resource for current and future scientific studies.

Read the detailed description

Glioblastoma multiforme (GBM) is the most common and lethal primary Brain and Spinal Tumor in adults. It is nearly uniformly fatal, with a median survival of approximately one year, despite modern treatment modalities. Efforts to understand why some patients live longer or shorter than the average may provide insights into the biology of these neoplasms. For years, researchers have tried to identify independent predictors that could help in treatment planning. With the recent interest in molecular biology and molecular genetics, tumor markers are now being examined as potential predictors. A marker that could predict tumor response to therapy, the likelihood of recurrence, and survival would thus be quite useful.

02

Conditions studied

  • Glioblastoma Multiforme
  • Glioma
  • Neuroectodermal Tumors

Keywords

  • Tissue Bank
  • Glioblastoma Multiforme
  • NAT2
  • EGFR
  • MGMT
  • Brain and Spinal TumorGliomas
03

In context

Glioblastoma

2,132 studies on the registry are indexed under Glioblastoma; 464 are open to participants now.

This study's planned enrollment of 70 is above the median of 60 across 208 observational studies indexed under Glioblastoma.

Browse Glioblastoma studies →

Lead sponsor

Taipei Medical University WanFang Hospital is the lead sponsor of 201 studies on the registry; 20 are open to participants now.

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

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Neurosurgery clinic or oncology clinic in Wan Fang Hospital

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients must have a suspected or confirmed diagnosis of Brain and Spinal Tumor
  • Age greater than 20
  • Signed consent

Exclusion criteria

Exclusion Criteria:

  • Known infection
  • Any other clinical condition which, in the opinion of the principal investigator, would not allow completion of this study
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
70 participants (estimated)
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Collect, annotate, and store fresh frozen specimens of normal tissue, tumors, and pre-malignant lesions for biological investigation.

    Time frame: 5 years

Secondary outcomes

  1. Collect, process, and store serum, plasma and isolate lymphocytes from blood drawn from patients with Brain and Spinal Tumor

    Time frame: 5 years

  2. Establish a database to link materials acquisition, pathologic, and clinical information on patients who participate in the protocol

    Time frame: 5 years

  3. To utilize the clinical database to perform clinical and pathological correlation with the results of current and future scientific studies

    Time frame: 5 years

  4. To evaluate various NAT2, EGFR and MGMT for evidence of genomic and biochemical activation

    Time frame: 5 years

  5. To test the effect of small molecule inhibitors on the activation of wild-type and mutant NAT2, EGFR, MGMT and/or other potential molecular targets

    Time frame: 5 years

  6. To correlate tumor genotype and signaling abnormalities with clinical response to NAT2, EGFR, MGMT and/or other potential molecular targets inhibitors

    Time frame: 5 years

  7. Analysis of laboratory findings in relationship to patient demographics and clinical course

    Time frame: 5 years

07

Study locations

1 of 1 sites recruiting
  • Taipei Medical University-Wan Fang Hospital
    Taipei, 116, Taiwan
    Recruiting
    • Kuo-Sheng Hung, MD, PhD · Contactkshung25@gmail.com · 886-2-2930-7930
    • Kuo-Sheng Hung, MD., Ph. D · Principal investigator
    • Wen-Ta Chiu, M.D., Ph. D · Sub investigator
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of May 2008, a primary completion of May 2013 and a completion of May 2013. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
May 26, 2008
First posted
May 29, 2008
Start
May 2008
Primary completionEst.
May 2013
CompletionEst.
May 2013
Last update
Apr 12, 2011
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 12, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00686387
First posted
May 29, 2008
Start date
May 2008
Primary completion
May 2013 (estimated)
Completion
May 2013 (estimated)
Last update
Apr 12, 2011

Study contacts

Kuo-Sheng Hung, M.D., Ph. D.
Contact
kshung25@gmail.com
886-2-2930-7930 ext. 6942
Kuo-Sheng Hung, MD, PhD
principal investigator · Taipei Medical University-Wan Fang Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2011. You cannot join it, but the record below documents what was studied.

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