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UV Sensor in Patients With Actinic Keratosis

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Almirall

Status

Completed

Conditions

Keratosis, Actinic

Treatments

Device: UV sensor

Study type

Observational

Funder types

Industry

Identifiers

NCT05481073
Usability UV sensor study

Details and patient eligibility

About

To validate the use of Ultraviolet (UV) radiation sensor in patients with actinic keratosis, to identify barriers to its use in prospective longitudinal studies.

Full description

To prevent both acute and chronic damage from exposure to UV A and UV B radiation. Personal UV exposure can be assessed by portable sensors. Having an accurate awareness of one's own behavior (assessed by the accuracy of the UV sensor), can motivate and engage with skin protection.

Enrollment

10 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

>=65 years presenting actinic keratosis on scalp and/or face

Exclusion criteria

Patients who, due to health problems or lifestyle habits, do not expose themselves regularly to UV radiation (outdoor) for at least one hour a day.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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