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OmegaChild - Omega-3 Supplementation to Children Previously Treated for Cancer (OmegaChild)

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ClinicalTrials.gov Identifier: NCT02134600
Recruitment Status : Completed
First Posted : May 9, 2014
Last Update Posted : August 28, 2018
Sponsor:
Collaborator:
Smartfish AS
Information provided by (Responsible Party):
Per Kogner, Karolinska Institutet

Brief Summary:
The purpose of this study is to find an optimal dose of omega-3 that can be given to children who have completed cancer therapy. The future aim is to add omega-3 to conventional cancer treatment modalities and thereby hopefully increase the treatment efficacy, which will have to be addressed in subsequent phase-2 studies.

Condition or disease Intervention/treatment Phase
Pediatric Cancer Dietary Supplement: Omega-3 enriched fruit juice Phase 1

Detailed Description:

The rationale for this phase-1 trial is to find an appropriate dose of omega-3 for future phase-2 studies. The investigators aim at defining a dose that can safely be given to children previously treated for cancer, and that does not cause unacceptable side effects. In a longer perspective, randomized control trials are planned where the supplement is given for longer periods of time, and in combination with conventional cancer treatment. In preparation for these trials, this dose finding study was designed that also evaluates compliance. Subsequently the investigators hope that this supplementation can be beneficial for children during both cancer treatment and after remission.

The study population consists of children judged to be in complete clinical remission from cancer. In a phase 1 trial, one usually uses healthy individuals as study subjects, but in pediatric studies this is not allowed. Therefore patients who are in full remission were chosen as study objects, but who still come to the clinic for regular follow-ups. This group of patients is relevant for this study since it represents all ages and base-line diets, all kinds of childhood cancers, and because they have suffered from cancer and in many cases still live with the severe consequences of it.

The study is designed to give five groups of eight individuals each different doses of omega-3 adjusted to body surface area. The first group starts out on a dose of omega-3 fatty acids that is similar to the generally recommended daily intake for adults (200-400 mg). A dose escalation is then done performed group wise. The highest possible dose in this study (2 x 3000mg/day at dose level 3000 mg/m2 to a child at 1.55 m2, 3871 mg/m2) is still lower than what has previously been given as maximum to children in other studies. The investigators will keep escalating the dose level within the study only as long as no unacceptable side effects are reported.

The administration is done orally by drinking 200 mL of omega-3 supplemented fruit juice daily. It has a good fruity taste, low amounts of sugar, and no fish flavour. This should facilitate treatment compliance for the children in particular compared to when omega-3 is given in capsules - the commonest choice in other studies, but less suitable for children. Compliance is important and not further jeopardized by trying to divide the fruit juice in less amounts than the whole package, but the individually prescribed dose as well as the actual amount ingested will be recorded and exact calculations used in the analysis of the study.

All study results are primarily evaluated on an intention-to-treat basis, but will also be calculated as treated per protocol and further calculated on the exact dose consumed over 90 days given the compliance in terms of consumed number of fruit juice packages.


Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 40 participants
Intervention Model: Single Group Assignment
Masking: Single (Participant)
Primary Purpose: Supportive Care
Official Title: OmegaChild - Omega-3 Supplementation to Children Now in Full Remission From a Previous Cancer; an Early Phase Dose-finding Study.
Actual Study Start Date : May 2014
Actual Primary Completion Date : August 2016
Actual Study Completion Date : September 2, 2016

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Omega-3 enriched fruit juice
Single arm study: Omega-3 enriched fruit juice in increasing dosage
Dietary Supplement: Omega-3 enriched fruit juice

Different doses of omega-3 will be administered to five different groups:

400, 800, 1200, 2400 and 3000 mg/m2.

Other Name: Nutrifriend by Smartfish AS




Primary Outcome Measures :
  1. Omega-3 index [ Time Frame: 3 months ]

    Omega-3 index is defined as % of DHA + EPA of total fatty acids in erythrocyte membranes.

    (DHA: Docosahexaenoic acid. EPA: Eicosapentaenoic acid).



Secondary Outcome Measures :
  1. Adverse Events [ Time Frame: 3 months ]
    Adverse events will be graded according to NCI Common Terminology Criteria for Adverse Events (CTCAE) v.4.


Other Outcome Measures:
  1. Compliance [ Time Frame: 3 months ]
    Compliance is calculated in percentage (%) using the number of fruit juice packages actually consumed (according to patient diary and interview) / number of packages prescribed (one or two daily pending dose level and body surface area).



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Ages Eligible for Study:   2 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. 2-18 years old
  2. Diagnosed with and now in complete clinical remission from any type of cancer
  3. Completed conventional therapy according to specific protocols within three years
  4. Spoken and written Swedish is understood by caregiver and/or child
  5. Expected to attend clinical follow-ups the coming three months.
  6. Performance Level: Karnofsky ≥ 60% for patients > 16 years of age and Lansky ≥ 60 for patients ≤16 years of age. Note: Neurologic deficits in patients with tumors of the CNS (central nervous system) must have been relatively stable for a minimum of 1 month prior to study enrollment. Patients who are unable to walk because of paralysis, but who are up in a wheelchair, will be considered ambulatory for the purpose of assessing the performance score.
  7. Written informed consent by all caregivers and if possible by the child after 7 years of age.

Exclusion Criteria:

  1. Known coagulation disorder
  2. Expected elective invasive surgery during the treatment
  3. Allergic to: fish or fish oil, protein from cow milk, fruit juice from any of the included fruits (apple, pear, pomegranate, passion fruit, peach, aronia)
  4. Supplementation of omega-3 during the last month
  5. Regular intake of NSAIDs (nonsteroidal antiinflammatory drugs), aspirin (ASA) or vitamin D
  6. Breastfeeding or pregnancy
  7. Participates in other clinical trials where results may be altered by additional intervention

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02134600


Locations
Sweden
Childhood Cancer Research Unit, Astrid Lindgren Children´s Hospital, Karolinska Institutet
Stockholm, Sweden, 17176
Sponsors and Collaborators
Per Kogner
Smartfish AS
Investigators
Principal Investigator: Per Kogner, Professor Karolinska Institutet