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Trial · NCT01534845

Efficacy Study of Radiotherapy Alone Versus CCRT With Temozolomide in Grade III Gliomas Without 1p/19q Codeletion

NCT01534845, Phase 2, Unknown, Jong Hoon Kim

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Efficacy Study of Radiotherapy Alone Versus CCRT With Temozolomide in Grade III Gliomas Without 1p/19q Codeletion. Trials, record NCT01534845. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01534845

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Efficacy Study of Radiotherapy Alone Versus CCRT With Temozolomide in Grade III Gliomas Without 1p/19q Codeletion
NCT number
NCT01534845
Status
Unknown
Phases
Phase 2
Enrollment
90 participants, actual
Lead sponsor
Jong Hoon Kim
Conditions
Anaplastic Glioma of Brain, Loss of Chromosomes 1p/19q
Interventions
Temozolomide (Temodal)
First posted
2012-02-17
Last updated
2015-07-09

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primary2-year progression free survival(PFS)Assessed and followed for the duration of hospital stay, an expected average of 3 monthsFinal primary end-point: 2 year PFS. Progression free survival(PFS) is defined as the time from randomization to progressive disease or death, which ever occurs earlier.
Secondary5-year overall survival (OS)assessed at 10 wks, 22 wks, 34 wks, and followed up every 4 months until documentation of death.final secondary end-point : 5-year OS. Overall survival is defined as the time from randomization to death, which ever occurs earlier.
Secondary5-year progression-free survival (PFS)assessed at 10 wks, 22 wks, 34 wks, and followed up every 4 months until documentation of disease progression or death.final end-point : 5-year PFS
SecondarySafety (adverse events)up to 5 years
SecondaryMethylation status of MGMTbaselineconfirmed by MS-PCR.
SecondaryIDH mutationbaseline

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT01534845

GET https://conductscience.org/api/trials/v1/NCT01534845/registered