Trial · NCT02564367
Feasibility Study of Adjuvant Treatment With S-1 in Patients After R0-Resection of Adenocarcinoma of the Stomach and Esophagogastric Junction
NCT02564367, Phase 1, Phase 2, Completed, AIO-Studien-gGmbH
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Feasibility Study of Adjuvant Treatment With S-1 in Patients After R0-Resection of Adenocarcinoma of the Stomach and Esophagogastric Junction. Trials, record NCT02564367. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02564367
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Feasibility Study of Adjuvant Treatment With S-1 in Patients After R0-Resection of Adenocarcinoma of the Stomach and Esophagogastric Junction
- NCT number
- NCT02564367
- Status
- Completed
- Phases
- Phase 1, Phase 2
- Enrollment
- 30 participants, actual
- Lead sponsor
- AIO-Studien-gGmbH
- Conditions
- Adenocarcinoma,Stomach, Adenocarcinoma, Esophagogastric Junction
- Interventions
- S-1
- First posted
- 2015-09-30
- Last updated
- 2021-04-29
- Other registries' IDs
- eudract:2014-004116-11
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | number of patients with discontinuation of S-1 due to intolerable adverse reactions | 12 months | |
| Secondary | One-year relapse-free survival rate | 12 months | Mo local relapse or distant metastases within one year after start of adjuvant treatment |
| Secondary | Relapse-free survival | 2 years | relapse-free survival until end of study |
| Secondary | Quality of life | 12 months | European Organisation for Research and Treatment of Cancer (EORTC) C30 questionnaires |
| Secondary | One-year survival rate | 1 years | |
| Secondary | Overall survival | 2 years | |
| Other | plasma concentration of Tegafur (FT) | 12 months | To evaluate the pharmacokinetics of FT |
| Other | plasma concentration of 5-Fluorouracil (5-FU) | 12 months | To evaluate the pharmacokinetics of 5-FU |
| Other | plasma concentration of Gimeracil (CDHP) | 12 months | To evaluate the pharmacokinetics of CDHP |
Source ClinicalTrials.gov
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.
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/NCT02564367
GET https://conductscience.org/api/trials/v1/NCT02564367/registered