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NOT YET RECRUITING
NCT06363201
NA

Effect and Safety of Ocoxin Oral Solution on the Quality of Life of Paediatric Patients With Advanced Stage Solid Tumours

Sponsor: Catalysis SL

View on ClinicalTrials.gov

Summary

Exploratory study to evaluate the effect and safety of the use of Ocoxin® oral solution on the quality of life of paediatric patients with advanced stage solid tumours.

Official title: Exploratory Study to Evaluate the Effect and Safety of the Use of Ocoxin Oral Solution on the Quality of Life of Paediatric Patients With Advanced Stage Solid Tumours

Key Details

Gender

All

Age Range

7 Years - 18 Years

Study Type

INTERVENTIONAL

Enrollment

40

Start Date

2024-04-28

Completion Date

2025-12-15

Last Updated

2024-04-12

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

Ocoxin Oral solution

Patients will receive one vial of Ocoxin® orally daily, preferably at the same time each day. The duration of treatment will depend on the chemotherapy schedule the patient will receive. Treatment with Ocoxin® will be from the start of oncospecific therapy until two weeks after the end of therapy.

Locations (1)

Hospital Escuela, Tegucigalpa (Honduras)

Tegucigalpa, Francisco Morazán Department, Honduras