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Trial · NCT01414608

Results by group100

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

OutcomeGroupCategoryValueSpreadUnits
Overall Survival Rate at 5 YearsStandard Chemoradiation7195% Confidence Interval 66 to 75Percentage of participants
Overall Survival Rate at 5 YearsStandard Chemoradiation With Adjuvant Chemotherapy7295% Confidence Interval 67 to 76Percentage of participants
Progression-free Survival Rate at 5 YearsStandard Chemoradiation6295% Confidence Interval 57 to 66Percentage of participants
Progression-free Survival Rate at 5 YearsStandard Chemoradiation With Adjuvant Chemotherapy6395% Confidence Interval 58 to 68Percentage of participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard ChemoradiationAbdominal pain13Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard Chemoradiation With Adjuvant ChemotherapyAbdominal pain14Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard ChemoradiationAlanine aminotransferase increased4Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard Chemoradiation With Adjuvant ChemotherapyAlanine aminotransferase increased2Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard ChemoradiationAllergic reaction/hypersensitivity1Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard Chemoradiation With Adjuvant ChemotherapyAllergic reaction/hypersensitivity2Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard ChemoradiationAlopecia0Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard Chemoradiation With Adjuvant ChemotherapyAlopecia1Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard ChemoradiationAnemia32Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard Chemoradiation With Adjuvant ChemotherapyAnemia64Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard ChemoradiationAspartate aminotransferase increased3Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard Chemoradiation With Adjuvant ChemotherapyAspartate aminotransferase increased2Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard ChemoradiationColitis2Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard Chemoradiation With Adjuvant ChemotherapyColitis2Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard ChemoradiationColonic obstruction1Participants
Number of Participants With Adverse Events (Grade 3 or Higher) in First YearStandard Chemoradiation With Adjuvant ChemotherapyColonic obstruction1Participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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