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Trial · NCT02296658

A Phase II Study of Postoperative S-1-Based Chemoradiotherapy in Gastric Cancer

NCT02296658, Phase 2, Unknown, Chinese Academy of Medical Sciences

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. A Phase II Study of Postoperative S-1-Based Chemoradiotherapy in Gastric Cancer. Trials, record NCT02296658. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02296658

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Trial

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

Title
A Phase II Study of Postoperative S-1-Based Chemoradiotherapy in Gastric Cancer
NCT number
NCT02296658
Status
Unknown
Phases
Phase 2
Enrollment
60 participants, estimated
Lead sponsor
Chinese Academy of Medical Sciences
Conditions
Stomach Neoplasms, Chemoradiotherapy, Adjuvant, Radiotherapy, Intensity-Modulated
Interventions
intensity-modulated radiotherapy, S-1
First posted
2014-11-20
Last updated
2014-11-20

Source ClinicalTrials.gov

Registered outcomes6

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

ListOutcomeTime frameDescription
PrimaryDisease free survival3 years
PrimaryLocoregional recurrence free survival3 years
PrimaryOverall survival3 years
PrimaryDistant metastasis free survival3 years
SecondaryChemoradiotherapy-induced toxicities assessed by CTCAE 4.0during treatment and within the first 30 days after completion of chemoradiotherapy
OtherComparison of dosimetric differences between radiation techniques1 yearTo compare the dosimetric differences between the volumetric-modulated arc therapy (VMAT), Tomotherapy and intensity-modulated radiotherapy (IMRT) techniques in treatment planning.

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/NCT02296658

GET https://conductscience.org/api/trials/v1/NCT02296658/registered