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Advanced Harmonic Generation Microscopy for Treatment Assessment of Cutaneous Pigmentary Disorder

Primary Purpose

Solar Lentigo, Nevus Zygomaticus

Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
HGM
Sponsored by
National Taiwan University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Solar Lentigo focused on measuring Solar Lentigo, Nevus Zygomaticus, Harmonic Generation Microscopy, In Vivo

Eligibility Criteria

20 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

1. Main inclusion criteria:

  1. Subjects are aged 20 to 85 years at Screening, and can be either sex.
  2. Subjects are Fitzpatrick skin type III or IV.
  3. Subjects must have been diagnosed to have solar lentigos or nevus zygomaticus, which are larger than 4 mm in diameter on both sides of the face.

2. Main exclusion criteria:

  1. Subjects have previous treatments on the solar lentigos or nevus zygomaticus.
  2. Subjects have a history of adverse reaction to laser treatments, including allergy to topical anesthesia application.
  3. Subjects have a history of chronic inflammatory disorder such as atopic dermatitis on the face.
  4. Subjects are pregnant or breast feeding.
  5. Subjects have frequent sun exposure (≥4 hours per day).

Sites / Locations

  • National Taiwan University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Solar lentigo

Nevus zygomaticus

Arm Description

25 Patients with Solar lentigo

25 Patients with Nevus zygomaticus

Outcomes

Primary Outcome Measures

25 participants with Solar Lentigo and 25 participants with Nevus zygomaticus as assessed by clinical photographs
The primary endpoint is the improvement of target at week 6 scored with a 7-grade. physician global assessment

Secondary Outcome Measures

25 participants with Solar Lentigo and 25 participants with Nevus zygomaticus as assessed by Harmonic Generation Microscopy.
The HGM system will be combined to provide the noninvasive microscopic images in SL and NZ sites during each follow-up for pathological diagnosis

Full Information

First Posted
June 10, 2018
Last Updated
May 4, 2020
Sponsor
National Taiwan University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03578315
Brief Title
Advanced Harmonic Generation Microscopy for Treatment Assessment of Cutaneous Pigmentary Disorder
Official Title
Advanced Harmonic Generation Microscopy for Treatment Assessment of Cutaneous Pigmentary Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
July 31, 2020 (Anticipated)
Study Completion Date
July 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this study, the investigators demonstrated that in vivo THG microscopy can differentiate Solar lentigos (SL), Nevus zygomaticus(NZ) and normal skin based on the optical nature of melanin. This THG-based procedure provides a valuable tool for noninvasive determination of third-order nonlinear susceptibility of melanin within the skin. It can also provide real-time histopathology information for treatment follow-up, without performing an invasive skin biopsy.
Detailed Description
A nonrandomized, controlled, split-face comparative study was conducted to compare the efficacy and safety between quality-switched ruby laser (QSRL) and 532-nm picosecond Nd:YAG laser (532-PSNYL for SL, 1064-PSNYL for NZ) in the treatment of solar lentigo clinically and histologically by harmonic generation microscopy (HGM). After baseline photography and in vivo harmonic generation microscopy (HGM) imaging, QSRL and 532-PSNYL or 1064-PSNYL therapy for solar lentigos and nevus zygomaticus on the left and right side of the face, respectively, were performed for each subject. The subjects underwent follow-up assessment at weeks 3 and 6. Statistical analysis: All data gathered went through decoding and were analyzed by blinded evaluators using SPSS software (version 20.0; IBM, Armonk, NY). All tests were two-sided. A P value of < .05 was considered to be statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Solar Lentigo, Nevus Zygomaticus
Keywords
Solar Lentigo, Nevus Zygomaticus, Harmonic Generation Microscopy, In Vivo

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Solar lentigo
Arm Type
Experimental
Arm Description
25 Patients with Solar lentigo
Arm Title
Nevus zygomaticus
Arm Type
Experimental
Arm Description
25 Patients with Nevus zygomaticus
Intervention Type
Device
Intervention Name(s)
HGM
Intervention Description
To Study the Efficacy and safety of QSRL and PSNYL in the Treatment of target: A nonrandomized, controlled, split-face comparative study
Primary Outcome Measure Information:
Title
25 participants with Solar Lentigo and 25 participants with Nevus zygomaticus as assessed by clinical photographs
Description
The primary endpoint is the improvement of target at week 6 scored with a 7-grade. physician global assessment
Time Frame
6 months
Secondary Outcome Measure Information:
Title
25 participants with Solar Lentigo and 25 participants with Nevus zygomaticus as assessed by Harmonic Generation Microscopy.
Description
The HGM system will be combined to provide the noninvasive microscopic images in SL and NZ sites during each follow-up for pathological diagnosis
Time Frame
1-2 hours per case

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
1. Main inclusion criteria: Subjects are aged 20 to 85 years at Screening, and can be either sex. Subjects are Fitzpatrick skin type III or IV. Subjects must have been diagnosed to have solar lentigos or nevus zygomaticus, which are larger than 4 mm in diameter on both sides of the face. 2. Main exclusion criteria: Subjects have previous treatments on the solar lentigos or nevus zygomaticus. Subjects have a history of adverse reaction to laser treatments, including allergy to topical anesthesia application. Subjects have a history of chronic inflammatory disorder such as atopic dermatitis on the face. Subjects are pregnant or breast feeding. Subjects have frequent sun exposure (≥4 hours per day).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yi-Hua Liao
Phone
0972651558
Email
yihualiao@ntu.edu.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yi-Hua Liao
Organizational Affiliation
National Taiwan University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Taiwan University Hospital
City
Taipei
ZIP/Postal Code
10002
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yi-Hua Liao
Phone
0972651558
Email
yihualiao@ntu.edu.tw

12. IPD Sharing Statement

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Advanced Harmonic Generation Microscopy for Treatment Assessment of Cutaneous Pigmentary Disorder

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