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Evaluation of effects of oral nutrition enriched with Eicosapentaenoic acid(EPA) in patients underwent neoadjuvant chemo therapy for head and neck cancer.

Evaluation of effects of oral nutrition enriched with Eicosapentaenoic acid(EPA) in patients underwent neoadjuvant chemo therapy for head and neck cancer. - Evaluation of effects of oral nutrition enriched with Eicosapentaenoic acid(EPA) in patients underwent neoadjuvant chemo therapy for head and neck cancer.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000007844
Enrollment
30
Registered
2012-05-01
Start date
2012-05-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head and neck cancer

Interventions

EPA-enriched oral nutrition of 2 packs and oral nutrition with EHA of 250ml was taken 6 to 7 weeks duraing neoadjuvant chemotherapy. oral nutrition with EHA of 250ml was taken 6 to 7 weeks duraing ne

Sponsors

Juntendo University school of medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.histologically daiagnosed SCC 2.patients had untreatement head and neck squamous cell carcinoma who needs neoadjuvant chemotherapy 3. ECOG PS of 0, 1 or 2 and the patients who can attend a hospital as a outpatient 4.Written informed consent 5.Sufficient oral or enteral intake 6.Confirmed by the following data white blood cell count 3000-9000/mm3. platelet count over 100,000/mm3. hemoglobin count over 9.0g/dl. serum creatinine below 1.2mg/dl. creatinine clearance over 60 ml/min

Exclusion criteria

Exclusion criteria: 1.with incurable other cancer 2.with obvious infectious disease 3.Uncontrollable diabetes mellitus 4.oral administration of steroid 5.with cardiac, liver, or renal failure 6.with allergy of milk and soybean 7.pregnant, lactating women or women of childbearing potential 8.with chronic inflammatory disease 9.lack of agreement 10.incidence of cerebral hemorrhage or subarachnoid hemorrhage within 1 month before registration 11.oral administration of EPA before registration

Design outcomes

Primary

MeasureTime frame
transition of nutritional condition and inflammatory reaction.

Secondary

MeasureTime frame
length of hostpitalization adverse event rate of completion for radical therapy survival rate

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026