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UV Sensor in Patients With Actinic Keratosis

NCT05481073 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2022-11-14

No results posted yet for this study

Summary

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

Conditions

  • Keratosis, Actinic

Interventions

DEVICE

UV sensor

Use of UV sensor to be informed about the sun exposure daily through a mobile application

Sponsors & Collaborators

  • Almirall, S.A.

    lead INDUSTRY

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-13
Primary Completion
2022-08-02
Completion
2022-09-01

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05481073 on ClinicalTrials.gov