Image Data Collection of Tanned Skin During Phototherapy Treatment Using a Multi-spectral Camera

Sponsor
Lumenis Be Ltd. (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05692544
Collaborator
(none)
10
5

Study Details

Study Description

Brief Summary

This is a prospective, observational, single-center, image collection study. Any patient who arrived at the phototherapy clinic for the first time, regardless of this study, and is prescribed a total of 30 treatments can be included, regardless of skin or medical condition.

After consenting subjects at least 5 close-up images will be taken from the specified anatomical areas, at different angles, using the SMART camera. Additional reference images of skin that is not exposed to the phototherapy treatment will be taken with the SMART Camera. Global image of the skin using a regular high-resolution camera is optional. The images will be collected on baseline visit, at least every 3 phototherapy treatments (approximately once a week), and at the last phototherapy treatment visit. i.e., in total of at least 11 phototherapy treatment visits. Follow-up images will be taken at 1-week and 2 weeks following the last phototherapy treatment.

Images shall be taken from any anatomical area that does not consist of any marked lesions or skin conditions. All images will be non-identifying.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Phototherapy treatment

Detailed Description

The SMART camera is advanced proprietary multi-spectral system camera, developed for research purposes. The SMART camera system is based on commercially available components and consists of 3 modules:

  1. Camera Handpiece- Spectral module with a monochromatic camera, optics, and an array of LEDs at 7 different wavelengths.

  2. Control Unit - an electronic box that powers and controls the camera. It includes electronics and a miniature computer.

  3. Touch screen monitor - With user interface to operate the system When taking a photo, a series of cross-polarized monochromatic images are taken, each at different illumination color (wavelength). In total, seven images are taken with blue (450nm), teal (490nm), lime (570nm), orange (590nm), red (660nm), IR-1 (730nm), IR-2 (860nm). The total acquisition time for the seven images is 0.1sec. The images are stored in a dedicated directory on a removable hard disk in the control unit in correlation to patient ID entered through the user interface on the laptop. The number of images that can be taken is unlimited.

The camera passed the following safety tests by certified lab:
  1. Check-up Safety Testing - IEC-60601-1 tests for investigational device by external laboratories according to IEC 60601-1, IEC 60601-2-22, IEC 60825-1, and IEC 60601-1-2 standards

  2. LED Hazard Evaluation UV, Visible & NIR Test, according to IEC62471 by an external certified laboratory

Study Design

Study Type:
Observational
Anticipated Enrollment :
10 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Image Data Collection of Tanned Skin During Phototherapy Treatment Using a Multi-spectral Camera
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Outcome Measures

Primary Outcome Measures

  1. Image data [4-months]

    Images will be collected through the study

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
    1. Any patient, male or female 18 years or older. 2. Patient is scheduled for 30 treatments or more of phototherapy 3. Subject is capable and willing to sign an informed consent 4. Subject is willing to comply with study schedule 5. Subject has areas of skin that do not consist any marked lesions, hairs or skin conditions and can be captured in the study
Exclusion Criteria:
    1. Subjects incapable of providing an informed consent

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Lumenis Be Ltd.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lumenis Be Ltd.
ClinicalTrials.gov Identifier:
NCT05692544
Other Study ID Numbers:
  • LUM-ABU-SMRT-22-03
First Posted:
Jan 20, 2023
Last Update Posted:
Jan 20, 2023
Last Verified:
Jan 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jan 20, 2023