Clinical trial · Interventional
COGNUTRIN in Breast Cancer Survivors
Pilot Clinical Trial of COGNUTRIN in Breast Cancer Survivors
NCT01823991CI-TRIAL-00045942completedEarly Phase 1Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to examine the safety and influence of an intervention (COGNUTRIN) using nutritional supplements (n-3 fatty acids and blueberry anthocyanins) on cognitive performance in breast cancer survivors following chemotherapy. The investigators' goal is to treat or lessen the late effects of cancer treatment. The supplement to be used will be a combination of the following: (1) VitaBlue (40% polyphenolics, 12.5% anthocyanins from blueberries (BB) and (2) n-3 fatty acids - Lovaza.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Lovaza® | Drug | — | UNRESOLVED |
| Placebo | Other | — | UNRESOLVED |
| VitaBlue™ | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- COGNUTRIN (VITABLUE and n-3 fatty acids)
- description
- Participants will be provided with two bottles containing Lovaza and VitaBlue. Participants will be asked to take 1 tablet of Lovaza two times a day and 1 tablet of VitaBlue three times a day.
- interventionNames
- Drug: VitaBlue™
- Drug: Lovaza®
- type
- PLACEBO_COMPARATOR
- label
- Placebo Administration
- description
- Participants will be provided with two bottles containing placebo. Participants will be asked to take 1 tablet of one placebo two times a day and 1 tablet of other placebo three times a day.
- interventionNames
- Other: Placebo
Primary outcomes (4)
- measure
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 40 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: * Cases with Stage II-IIIA Breast Cancer that have completed adjuvant treatment with anthracyclines and/or taxanes + or -Radiation therapy within past 6 months(+/- 7 days) (subjects on concurrent endocrine therapy (TAM, Aromatase inhibitors are also eligible to participate as this is standard of care for this patient population) * Able to understand and sign the informed consent * Fluent in reading, comprehension and communication in the English language * No evidence of dementia - Mini Mental State Examination (MMSE) \>=23 but some evidence of cognitive impairment * Must be aware of the nature of his current medical condition and must be willing to give consent after being informed of the experimental nature of therapy, alternatives, potential benefits, side-effects, risks and discomforts * Eastern Cooperative Oncology Group (ECOG) performance status of 0- 2 (Karnofsky score \>60%) * Acceptable hemoglobin and hematocrit level based on complete blood count (CBC) * Must be willing to be monitored for adequacy of nutritional intake during the intervention, as is the current standard of clinical practice Exclusion Criteria: * Use of estrogens (oral, dermal or vaginal), progesterone (oral or topical), androgens, Raloxifene or Tamoxifen during the previous 3 months * Use of over the counter steroid hormonal supplements including dehydroepiandrosterone (DHEA) * Patients with advanced or Stage IIIIB or IV breast cancer or other cancers * Use of n-3 fatty acids or high dose antioxidant supplements other than what is provided in the trial * History of known allergy to components of the study supplements * Renal or liver disease * Concurrent participation in another chemoprevention trial * Evidence of bleeding diathesis or coagulopathy * Metabolic abnormalities (e.g. thyroid disorders, insulin dependent diabetes, rheumatologic disease etc.) * Known claustrophobia, presence of pacemaker and/or ferromagnetic material in their body that would prohibit MRI imaging * Medical history of concussions * Other acute or chronic medical or psychiatric condition or laboratory abnormality that may increase risk associated with study participation or study drug administration, or may interfere with interpretation of study results, and in the judgment of the investigator would make the potential participant inappropriate for entry into this study
References
Publications (0)
Data not yet available
No reference posted for this study.