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Clinical Trials/RPCEC00000281
RPCEC00000281
Not yet recruiting
Phase 2

Evaluation of the effect of the nutritional supplement Oncoxin®-Viusid® on the quality of life of patients with advanced pancreatic adenocarcinoma. Phase II.

aboratories Catalysis, S.A0 sites30 target enrollmentAugust 1, 2018

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Pancreatic cancer
Sponsor
aboratories Catalysis, S.A
Enrollment
30
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 1, 2018
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
aboratories Catalysis, S.A

Eligibility Criteria

Inclusion Criteria

  • 1\- Patients of any sex, resident in Cuba, with an age greater than or equal to 18 years.
  • 2\- Patients that meet the diagnostic criteria.
  • 3\- Patients with general health according to Karnofsky \=70%.
  • 4\- Life expectancy greater than or equal to 3 months.
  • 5\- Patients eligible to receive chemotherapy.
  • 6\- Patients who have signed the informed consent.
  • 7\- Patients who have laboratory values in parameters that do not contraindicate the administration of chemotherapy: Hemoglobin \= 90 g/l, Total Leukocyte Count \= 3\.0 x 109 / L, Absolute Neutrophil Count \=1\.5 x 109 / L. o Platelet count \=100 x 109 / L, Total bilirubin values \= 1\.5 times the upper limit of the normal range established in the institution, TGO and TGP values \=2\.5 times the upper limit of the normal interval established in the institution and, Creatinine values within the normal limits of the institution.

Exclusion Criteria

  • 1\- Patients who are receiving another product under investigation.
  • 2\- Patients with known hypersensitivity to any of the active ingredients of the chemotherapy used
  • 3\- Patients with decompensated intercurrent diseases, including: HBP, Diabetes Mellitus, Ischemic Heart Disease, active infections, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, liver damage or any other special condition that at the discretion of the doctor puts their health at risk and his life during the study or his participation in the trial.
  • 4\-Patients who are pregnant or breastfeeding.
  • 5\- Patients with mental disorders that could limit adherence to the requirements of the clinical trial and may hinder the collection of information, treatment or follow\-up.
  • 6\- Patients with brain metastases.

Outcomes

Primary Outcomes

Not specified

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