Skip to content

The efficacy testing of a Glu-Cer against adverse skin event

Protective effect with Glu-Cer intake against adverse skin event of chemoradiotherapy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs061190040
Enrollment
30
Registered
2020-03-16
Start date
2020-11-19
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 Head and Neck cancer

Interventions

Treatment with dietary glucosylceramide

Sponsors

Fujiwara Kazunori
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Origin of the cancer: maxillary, oral cavity, pharynx, larynx, cervical esophagus Recieve chemoradiation against head and neck cancer Over 20 years old Enable to take a medicine orally Patient with bone marrow, and/or hepatic, and/or renal insufficiency within 14 days before starting of a trial Sign a consent form on one's own

Exclusion criteria

Exclusion criteria: Konjac allergy Prominent symptom at the site of a skin test Patient who had chronic skin disorder like collagen diseases and take medication regularly Remain under other scrutiny, or within 3 months after finishing other clinical trial Asthma patients Take antihistamine medicine At risk of becoming pregnant and breast-feeding woman

Design outcomes

Primary

MeasureTime frame
degree of the adverse event for the radiation field

Secondary

MeasureTime frame
Pain, degree, onset, and course of the adverse skin event Amount of the sphingolipids at the skin Evaluation of the skin function about transpiration rate, amount of moisture, and range of erythema and macule Adverse event, side effect

Contacts

Public ContactKazunori Fujiwara

Tottori University Hospital

kfujiwa@tottori-u.ac.jp+81-859-38-6627

Outcome results

None listed

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