Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 10:46 PM
Ignite Modification Date:
2025-12-26 @ 10:46 PM
NCT ID:
NCT02978612
Eligibility Criteria:
Inclusion Criteria:
* Radical surgery (R0/R1) for colon cancer
* Histologically verified adenocarcinoma of the colon
* Histologically verified lymph node metastases (Stage III)
* Age ≥ 75 years
* Able to undergo ambulatory treatment (adequate physical and mental function)
* Signed informed consent and expected cooperation of the patients for the treatment and follow up must be obtained and documented according to The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH GCP) and national regulations.
Exclusion Criteria:
* Distant metastases (stage IV)
* Frail according to geriatric assessment
* Significant cardiovascular disease (congestive heart failure, symptomatic coronary artery disease and cardiac dysrhythmia) or myocardial infarction within the past 12 months
* Previous treatment with chemotherapy for colorectal cancer
* Metastatic disease from other cancer
* Reduced cognitive function not enabling ability to give informed consent or compliance with the study
* History of prior or concurrent malignant neoplasm other than colorectal adenocarcinoma within the past five years, except curatively treated non-melanoma skin cancer or in situ carcinoma of the cervix
* Adverse reactions or hypersensitivity to capecitabine or related drugs and/or its excipients. Need to use medications contraindicated according to SmPC of the IMP(s), such as sorivudine, brivudin or chemically related compounds. Any other contraindication listed on the summary of product characteristics (SmPC) of the investigational medicinal Product (IMP)
* Use of methotrexate or other cytotoxic drugs as treatment of rheumatoid arthritis or other inflammatory disease and where it is considered contraindicated to stop this medication
* Known dihydropyrimidine dehydrogenase (DPD) deficiency
* Any reason why, in the opinion of the investigator, the patient should not participate
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
75 Years
Study:
NCT02978612
Study Brief:
Protocol Section:
NCT02978612