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Study on the utility of the short wavelength cut filter attached to the UVA 1(340~400nm) phototherapy device for Cutaneous T-cell Lymphomas.

Study on the utility of the short wavelength cut filter attached to the UVA 1(340~400nm) phototherapy device for Cutaneous T-cell Lymphomas. - Study on the utility of the short wavelength cut filter attached to the UVA 1(340~400nm) phototherapy device for CTCL.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038988
Enrollment
10
Registered
2019-12-28
Start date
2019-12-09
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

Cutaneous T-Cell Lymphomas

Interventions

attached the short wavelength cut filter not attached the short wavelength cut filter

Sponsors

Nagoya City University Graduate School of Medical Sciences Department of Geriatric and Environmental Dermatology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1 Cutaneous T-cell Lymphomas patients who are candidates for phototherapy. 2 Age between 16 and 65,written approval of patient. If the patient is a minor, the consent is needed from both the patient and the legal representative. 3 Patients who can understand the study and can issue consent to the study in writing.

Exclusion criteria

Exclusion criteria: 1 Patient who is not candidates for phototherapy. - Patient who will activate or recur malignant skin tumors. - Patient who has high carcinogenic risk(xeroderma pigmentosum, radiation therapy, internal use or touching career of arsenic etc.) - Patient who has remarkable photodermatosis(hereditary photodermatosis, albinism, porphyria, photosensitive collagen disease etc.) 2 Patient who participated other clinical studies or trials within 3 months of this study entry. 3 Pregnant or possibly pregnant women, or breastfeeding women. Women who wish to become pregnant during study participation. 4 Patient who is judged inappropriate to participate in the study by the investigator.

Design outcomes

Primary

MeasureTime frame
skin pigmentation of irradiation area

Countries

Japan

Contacts

Public ContactAkimichi Morita

Nagoya City University Graduate School of Medical Sciences Department of Geriatric and Environmental Dermatology

amorita@med.nagoya-cu.ac.jp052-853-8261

Outcome results

None listed

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