Skip to content

Evaluation of efficacy of improved nutrition for patients with head and neck cancer underwent oral nutritional supplements.

Evaluation of efficacy of improved nutrition for patients with head and neck cancer underwent oral nutritional supplements. - Evaluation of efficacy of improved nutrition for patients with head and neck cancer underwent oral nutritional supplements.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009348
Enrollment
30
Registered
2012-11-17
Start date
2012-11-19
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

RACOL-NF Liquid for Enteral Use

Sponsors

Kanazawa Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who will receive any one of the following 3 therapies: chemotherapy, radiation therapy, or chemoradiotherapy. 2.Patients who have been diagnosed and informed of diagnosis with head and neck cancer. 3.Patients who have been judged to be a candidate of oral intake by the investigator. 4.Patients aged 20 years old and older and 75 years old and under. 5.Patients and legal representative who have given voluntary written informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients who have a history of hypersensitivity to enteral nutritional supplements. 2.Patients with ileus. 3.Patients without an enteric function. 4.Patients with severe liver failure and/or renal failure. 5.Patients with abnormal glucose metabolism such as severe diabetes. 6.Patients with inborn error of amino acid metabolism. 7.Patients who had blood transfusion within one month. 8.Patients with active infection. 9.Patients with severe organ failure. 10.Patients who have edema at the time of registration. 11.Patients with electric implantable devices such as pacemakers. 12.Patients who are pregnant, suspected to be pregnant or breastfeeding. 13.Patients judged to be inappropriate for the study by the investigator.

Design outcomes

Primary

MeasureTime frame
Rate of change of body weight. Dose of oral nutritional supplements per body weight.

Countries

Japan

Contacts

Public ContactKanako Teraguchi

Kanazawa Medical University Department of Otorhinolaryngology-Head and Neck Surgery

kanako-y@kanazawa-med.ac.jp076-286-2211

Outcome results

None listed

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