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Spots Global Cancer Trial Database for Evaluation of Ocoxin®-Viusid® in Metastatic Colorectal Adenocarcinoma

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Trial Identification

Brief Title: Evaluation of Ocoxin®-Viusid® in Metastatic Colorectal Adenocarcinoma

Official Title: Evaluation of the Effect of the Ocoxin®-Viusid® Nutritional Supplement on the Quality of Life of Patients With Metastatic Colorectal Adenocarcinoma. Phase II

Study ID: NCT03559543

Interventions

Ocoxin-Viusid

Study Description

Brief 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.

Detailed 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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

National Institute of Oncology and Radiobiology (INOR), Havana, , Cuba

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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