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Clinical Trial Summary

The research product, registered as a nutritional supplement (Ocoxin®, oral solution), manufactured by Laboratorios Catalysis S. L., comes in the form of single-dose vials of 30 ml. It will be used at a rate of 60 ml daily (1 vial every 12 hours). Our main objective is To evaluate the effect of Ocoxin®-Viusid® on the quality of life of patients with metastatic colorectal adenocarcinoma. Our hypothesis is that the administration of the nutritional supplement Ocoxin®-Viusid® it is expected to improve the quality of life and enhance tolerance to chemotherapy in at least 70% of patients.


Clinical Trial Description

- To evaluate the effect of Ocoxin®-Viusid® on the quality of life of patients. - To evaluate the influence of Ocoxin®-Viusid® on tolerance to onco-specific therapy. - Identify the changes that occur in the nutritional status of patients receiving the supplement. - To evaluate the toxicity of Ocoxin®-Viusid® in combination with chemotherapy in patients with metastatic colorectal adenocarcinoma. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03559543
Study type Interventional
Source Catalysis SL
Contact
Status Completed
Phase Phase 2
Start date October 25, 2018
Completion date January 15, 2024

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