- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04519736
Single Band vs. Dual Band Pulsed Light Technology for the Treatment of Photodamage - A Split Face Comparison Study
Single Band (Alma) vs. Dual Band (Palomar) Pulsed Light Technology for the Treatment of Photodamage - a Split Face Comparison Study
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New Jersey
-
Hackensack, New Jersey, United States, 07601
- Skin Laser & Surgery Specialists of NY/NJ
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
The following are requirements for a potential subject's inclusion into the study:
- Male or female in good general health between 35 to 65 years of age.
- Must be willing to execute informed consent. Patient must also consent to having photos taken at each visit.
- A potential subject must exhibit:
Clinical diagnosis of photo damage affecting the face.
- For FEMALE PATIENTS OF CHILDBEARING POTENTIAL, must have had a regular menstrual cycle prior to study entry (a female is considered of childbearing potential unless she is postmenopausal, without a uterus and/or both ovaries, or has had a bilateral tubal ligation) and is willing to use an acceptable form of birth control during the entire course of the study [i.e., acceptable methods of birth control are oral contraceptives, contraceptive patches/rings/implants Norplanit®, Depo-Provena®, double-barrier methods (e.g. condoms and spermicide), abstinence and vasectomies of partner with a documented second acceptable method of birth control should the subject become sexually active]. All systemic birth control measures must be in consistent use at least 30 days prior to study participation.
- Must be willing to comply with study visits and complete the entire course of the study.
Exclusion Criteria:
Subjects meeting any of the following criteria will be excluded from participation:
The following are exclusion criteria for subjects in this study:
- A subject that underwent a laser / light treatment on the face within 12 months, or any topical treatment on the face within 6 months.
- A subject with any UNCONTROLLED systemic disease. A potential subject in whom therapy for a systemic disease is not yet stabilized will not be considered for entry into the study.
- A subject with a significant history or current evidence of a medical, psychological or other disorder that, in the investigator's opinion, would preclude enrollment into the study.
- A subject using any topical product containing a retinoid, retinol, or other vitamin A derivative within 3 months prior to or during the study period.
- A subject using any systemic steroid therapy within 6 months prior to or during the study period.
- A subject that has been treated with Botox/Dysport or filler/biostimulatory molecule injections to his/her face within the past 6 months.
- A subject using any topical medicated creams, lotions, powders, etc. on the treatment areas during the study period, other than the study treatment regimen within 14 days.
- A subject that has previously been treated with systemic retinoids within the past year (e.g., Accutane®, Roche Dermatologics).
- A subject with recently excessive facial exposure to sunlight or artificial UV light (e.g.: use of tanning beds/booths and/or sunbathing). During the study, when excessive sun exposure is unavoidable, subjects must wear appropriate protective clothing (e.g. hat, collar) and comply with the study dosing regimen of daily application of the dispersed sunblock.
- A subject with a recent history or active presence of any facial skin condition/disease that might interfere with the diagnosis or evaluation of study parameters (i.e. moderate to severe acne vulgaris, atopic dermatitis, psoriasis, rosacea, seborrheic dermatitis, excessive facial hair or coloration).
- A female subject who is pregnant, nursing an infant or planning a pregnancy during the study [throughout the course of the study, women of child-bearing potential must use reliable forms of contraception (i.e., oral contraceptive, intrauterine device, abstinence, or spermicides and condoms used in combination)].
- Current participation or participation within 30 days prior to the start of this study in a drug or other investigational research study.
Subjects who are pregnant, breast-feeding, or planning a pregnancy. Females of childbearing potential, must be either:
- using the same form (i.e. brand) and dosage regimen of an oral contraceptive pill or of a hormonal implant continuously for 3 months prior to study entry and continue during the entire study, or
- willing to use a different form of birth control during the study other than any form of hormonal methods such as oral contraceptive pills and hormonal implants 30 day prior to study entry and during the entire study period. For the purpose of this study, the following are also considered acceptable methods of birth control: double-barrier methods (e.g.: condoms and spermicide), abstinence and vasectomies of partner with a documented second acceptable method of birth control, should the subject become sexually active.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Harmony Dye-VL 500-600nm
The left side of the face will be treated with the Single Band Alma Harmony Dye-VL 500-600nm device.
Three treatments, administered in intervals of 21 +/- 2 days.
Each full face treatment duration will be approximately 20-30 minutes .
|
|
Active Comparator: Palomar MaxG
Right side of the face will be treated with the Dual Band Palomar MaxG device.
Three treatments, administered in intervals of 21 +/- 2 days.
Each full face treatment duration will be approximately 20-30 minutes .
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Photodamage
Time Frame: The investigator will evaluate the change in visual appearance of the treated area at 3 week, 6 week, 9 week treatments and before follow-up visit (3 months after the last treatment)
|
Investigator Evaluation of Specific Signs of Photo Damage The investigator will evaluate the clinical improvement from the visual appearance of the treated area and from the fixed magnification clinical photographs according to the following Global Assessment scale (compared to baseline photographs): Global Aesthetic Improvement Scale (GAIS ) Rating Description
|
The investigator will evaluate the change in visual appearance of the treated area at 3 week, 6 week, 9 week treatments and before follow-up visit (3 months after the last treatment)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Photodamage
Time Frame: Investigator will evaluate the change in visual appearance of the treated area at 3 week, 6 week, 9 week treatments, and before follow up visit (three months after the last visit)
|
Investigator Evaluation of Specific Signs of Photo Damage In addition, the Investigator will at each visit complete the Investigator Evaluation of Specific Signs of Photo Damage as seen below (for each of the handpieces): Poilikoderma of Civatte
Telangiectasias
Pigmented components of Photo Damage
|
Investigator will evaluate the change in visual appearance of the treated area at 3 week, 6 week, 9 week treatments, and before follow up visit (three months after the last visit)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- ALMA-500600-PL12DG
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Photodamage
-
Federal University of São PauloUnknown
-
Galderma Brasil Ltda.CompletedPhotoaging | PhotodamageBrazil
-
Alma Lasers Inc.Completed
-
AllerganCompleted
-
Fundación DermabaseIPS Universitaria-Universidad de Antioquia; Grupo de Investigacion Dermatologica...CompletedFacial PhotodamageColombia
-
ConBio, a Cynosure CompanyCompletedAcne Scars | Photodamage | Irregular PigmentationUnited States
-
Massachusetts General HospitalTerminatedActinic Keratosis | Extensive Photodamage | History of Numerous Skin CancersUnited States
Clinical Trials on Single Band vs. Dual Band Pulsed Light Technology for the Treatment of Photodamage
-
Norwegian Institute of Public HealthUniversity of Oslo; Oslo University Hospital; Oslo MunicipalityActive, not recruitingHip Fractures | Fall Injury