Skip to main content
Top
Published in: Trials 1/2019

Open Access 01-12-2019 | Phototherapy | Study protocol

A single-blind, dose-escalation, phase I study of high-fluence light-emitting diode-red light on Caucasian non-Hispanic skin: study protocol for a randomized controlled trial

Authors: Erica B. Wang, Ramanjot Kaur, Julie Nguyen, Derek Ho, Evan Austin, Emanual Maverakis, Chin-Shang Li, Samuel T. Hwang, R. Rivkah Isseroff, Jared Jagdeo

Published in: Trials | Issue 1/2019

Login to get access

Abstract

Background

Visible light (400 to 700 nm) is common in our environment, comprising 44% of total solar radiation and a large component of environmental light exposure. The effects of visible light on skin remain undefined. The red light portion of the visible spectrum (600 to 700 nm) may be used to treat skin diseases as a monotherapeutic modality or in combination with other agents. Light-emitting diode-red light (LED-RL) phototherapy may represent an important advance in light-based treatment modalities because it is non-invasive, inexpensive, portable, and easily combinable with other therapies. We previously determined the maximum tolerated dose (MTD) of high-fluence LED-RL (HF-LED-RL) in skin of color individuals to be 320 J/cm2. To the best of our knowledge, no clinical trials have been performed to determine the safety of higher doses of HF-LED-RL in Caucasian non-Hispanic individuals. The aim of this study is to investigate the safety of HF-LED-RL at doses of 480 and 640 J/cm2 in healthy Caucasian non-Hispanic individuals.

Methods

This is a single-blind, dose-escalation, randomized, controlled, phase I trial titled Safety Trial Assessing Red-light on Skin (STARS) 2. Healthy subjects will be randomly assigned to groups of five (three subjects randomly assigned to HF-LED-RL phototherapy and two subjects randomly assigned to mock therapy). Subjects in group 1 will receive HF-LED-RL or mock irradiation at the starting dose of 480 J/cm2, and the dose will be escalated in the subsequent group (group 2) to 640 J/cm2. The MTD is defined as the dose level below the dose at which two or more subjects (>20% of the cohort) experience a dose-limiting toxicity (DLT). After either the MTD is established or the study endpoint of 640 J/cm2 is achieved, additional HF-LED-RL phototherapy subjects and mock therapy subjects will be enrolled at that fluence (group 3) for a total number of up to 60 subjects. Each subject will receive a total of nine irradiation sessions, three times per week for three consecutive weeks.

Discussion

This follow-up study aims to provide important knowledge about safety and cutaneous effects of HF-LED-RL phototherapy of 480 and 640 J/cm2 in Caucasian non-Hispanic subjects. The importance of this clinical trial is that it may establish new treatment paradigms and a safety profile for LED-RL based on race and ethnicity.

Trial registration

ClinicalTrials.gov Identifier: NCT03433222. Registered on February 1, 2018 - Retrospectively registered.
Protocol date and version: January 12, 2018; version 1.
Appendix
Available only for authorised users
Literature
1.
go back to reference Pidwirny M. In: Pidwirny M, editor. Solar Radiation and Earth, in Understanding Physical Geography. British Columbia: Our Planet Earth Publishing; 2017. Pidwirny M. In: Pidwirny M, editor. Solar Radiation and Earth, in Understanding Physical Geography. British Columbia: Our Planet Earth Publishing; 2017.
3.
go back to reference Porges SB, Kaidbey KH, Grove GL. Quantification of visible light-induced melanogenesis in human skin. Photodermatol. 1988;5:197–200.PubMed Porges SB, Kaidbey KH, Grove GL. Quantification of visible light-induced melanogenesis in human skin. Photodermatol. 1988;5:197–200.PubMed
4.
go back to reference Soleymani T, Cohen DE, Folan LM, Okereke UR, Elbuluk N, Soter NA. Disparity in Cutaneous Pigmentary Response to LED vs Halogen Incandescent Visible Light: Results from a Single Center, Investigational Clinical Trial Determining a Minimal Pigmentary Visible Light Dose. J Drugs Dermatol. 2017;16:1105–10.PubMed Soleymani T, Cohen DE, Folan LM, Okereke UR, Elbuluk N, Soter NA. Disparity in Cutaneous Pigmentary Response to LED vs Halogen Incandescent Visible Light: Results from a Single Center, Investigational Clinical Trial Determining a Minimal Pigmentary Visible Light Dose. J Drugs Dermatol. 2017;16:1105–10.PubMed
5.
go back to reference Sklar LR, Almutawa F, Lim HW, Hamzavi I. Effects of ultraviolet radiation, visible light, and infrared radiation on erythema and pigmentation: a review. Photochem Photobiol Sci. 2013;12:54–64.CrossRef Sklar LR, Almutawa F, Lim HW, Hamzavi I. Effects of ultraviolet radiation, visible light, and infrared radiation on erythema and pigmentation: a review. Photochem Photobiol Sci. 2013;12:54–64.CrossRef
6.
go back to reference Mahmoud BH, Ruvolo E, Hexsel CL, Liu Y, Owen MR, Kollias N, et al. Impact of long-wavelength UVA and visible light on melanocompetent skin. J Invest Dermatol. 2010;130:2092–7.CrossRef Mahmoud BH, Ruvolo E, Hexsel CL, Liu Y, Owen MR, Kollias N, et al. Impact of long-wavelength UVA and visible light on melanocompetent skin. J Invest Dermatol. 2010;130:2092–7.CrossRef
7.
go back to reference Campbell SM, Tyrrell J, Marshall R, Curnow A. Effect of MAL-photodynamic therapy on hypertrophic scarring. Photodiagn Photodyn Ther. 2010;7:183–8.CrossRef Campbell SM, Tyrrell J, Marshall R, Curnow A. Effect of MAL-photodynamic therapy on hypertrophic scarring. Photodiagn Photodyn Ther. 2010;7:183–8.CrossRef
8.
go back to reference Nie Z, Bayat A, Behzad F, Rhodes LE. Positive response of a recurrent keloid scar to topical methyl aminolevulinate-photodynamic therapy. Photodermatol Photoimmunol Photomed. 2010;26:330–2.CrossRef Nie Z, Bayat A, Behzad F, Rhodes LE. Positive response of a recurrent keloid scar to topical methyl aminolevulinate-photodynamic therapy. Photodermatol Photoimmunol Photomed. 2010;26:330–2.CrossRef
9.
go back to reference Sakamoto FH, Izikson L, Tannous Z, Zurakowski D, Anderson RR. Surgical scar remodelling after photodynamic therapy using aminolaevulinic acid or its methylester: a retrospective, blinded study of patients with field cancerization. Br J Dermatol. 2012;166:413–6.CrossRef Sakamoto FH, Izikson L, Tannous Z, Zurakowski D, Anderson RR. Surgical scar remodelling after photodynamic therapy using aminolaevulinic acid or its methylester: a retrospective, blinded study of patients with field cancerization. Br J Dermatol. 2012;166:413–6.CrossRef
10.
go back to reference Li Y, Zhang J, Xu Y, Han Y, Jiang B, Huang L, et al. The Histopathological Investigation of Red and Blue Light Emitting Diode on Treating Skin Wounds in Japanese Big-Ear White Rabbit. PLoS One. 2016;11:e0157898.CrossRef Li Y, Zhang J, Xu Y, Han Y, Jiang B, Huang L, et al. The Histopathological Investigation of Red and Blue Light Emitting Diode on Treating Skin Wounds in Japanese Big-Ear White Rabbit. PLoS One. 2016;11:e0157898.CrossRef
11.
go back to reference Mamalis A, Jagdeo J. Light-emitting diode-generated red light inhibits keloid fibroblast proliferation. Dermatol Surg. 2015;41:35–9.CrossRef Mamalis A, Jagdeo J. Light-emitting diode-generated red light inhibits keloid fibroblast proliferation. Dermatol Surg. 2015;41:35–9.CrossRef
12.
go back to reference Mamalis A, Koo E, Garcha M, Murphy WJ, Isseroff RR, Jagdeo J. High fluence light emitting diode-generated red light modulates characteristics associated with skin fibrosis. J Biophotonics. 2016;9:1167–79.CrossRef Mamalis A, Koo E, Garcha M, Murphy WJ, Isseroff RR, Jagdeo J. High fluence light emitting diode-generated red light modulates characteristics associated with skin fibrosis. J Biophotonics. 2016;9:1167–79.CrossRef
14.
go back to reference Wunsch A, Matuschka K. A controlled trial to determine the efficacy of red and near-infrared light treatment in patient satisfaction, reduction of fine lines, wrinkles, skin roughness, and intradermal collagen density increase. Photomed Laser Surg. 2014;32:93–100.CrossRef Wunsch A, Matuschka K. A controlled trial to determine the efficacy of red and near-infrared light treatment in patient satisfaction, reduction of fine lines, wrinkles, skin roughness, and intradermal collagen density increase. Photomed Laser Surg. 2014;32:93–100.CrossRef
15.
go back to reference Archier E, Devaux S, Castela E, Gallini A, Aubin F, Le Maître M, et al. Carcinogenic risks of psoralen UV-A therapy and narrowband UV-B therapy in chronic plaque psoriasis: a systematic literature review. J Eur Acad Dermatol Venereol. 2012;26(Suppl 3):22–31.CrossRef Archier E, Devaux S, Castela E, Gallini A, Aubin F, Le Maître M, et al. Carcinogenic risks of psoralen UV-A therapy and narrowband UV-B therapy in chronic plaque psoriasis: a systematic literature review. J Eur Acad Dermatol Venereol. 2012;26(Suppl 3):22–31.CrossRef
16.
go back to reference Bolognia J, Schaffer J. Irradiation of skin with visible light induces reactive oxygen species and matrix-degrading enzymes. In: Bolognia J, Jorizzo J, Schaffer J, editors. Dermatology. 3rd ed; 2012. Bolognia J, Schaffer J. Irradiation of skin with visible light induces reactive oxygen species and matrix-degrading enzymes. In: Bolognia J, Jorizzo J, Schaffer J, editors. Dermatology. 3rd ed; 2012.
17.
go back to reference Jagdeo JR, Adams LE, Brody NI, Siegel DM. Transcranial red and near infrared light transmission in a cadaveric model. PLoS One. 2012;7:e47460.CrossRef Jagdeo JR, Adams LE, Brody NI, Siegel DM. Transcranial red and near infrared light transmission in a cadaveric model. PLoS One. 2012;7:e47460.CrossRef
18.
go back to reference Posadzki P, Car J. Light therapies for acne. JAMA Dermatol. 2018;154:597–8.CrossRef Posadzki P, Car J. Light therapies for acne. JAMA Dermatol. 2018;154:597–8.CrossRef
19.
go back to reference Fitzpatrick TB. The validity and practicality of sun-reactive skin types I through VI. Arch Dermatol. 1988;124:869–71.CrossRef Fitzpatrick TB. The validity and practicality of sun-reactive skin types I through VI. Arch Dermatol. 1988;124:869–71.CrossRef
20.
go back to reference Eilers S, Bach DQ, Gaber R, Blatt H, Guevara Y, Nitsche K, et al. Accuracy of self-report in assessing Fitzpatrick skin phototypes I through VI. JAMA Dermatol. 2013;149:1289–94.CrossRef Eilers S, Bach DQ, Gaber R, Blatt H, Guevara Y, Nitsche K, et al. Accuracy of self-report in assessing Fitzpatrick skin phototypes I through VI. JAMA Dermatol. 2013;149:1289–94.CrossRef
21.
go back to reference Jackson BA. Lasers in ethnic skin: a review. J Am Acad Dermatol. 2003;48(6 Suppl):S134–8.CrossRef Jackson BA. Lasers in ethnic skin: a review. J Am Acad Dermatol. 2003;48(6 Suppl):S134–8.CrossRef
22.
go back to reference Ho D, Kraeva E, Wun T, Isseroff RR, Jagdeo J. A single-blind, dose escalation, phase I study of high-fluence light-emitting diode-red light (LED-RL) on human skin: study protocol for a randomized controlled trial. Trials. 2016;17:385.CrossRef Ho D, Kraeva E, Wun T, Isseroff RR, Jagdeo J. A single-blind, dose escalation, phase I study of high-fluence light-emitting diode-red light (LED-RL) on human skin: study protocol for a randomized controlled trial. Trials. 2016;17:385.CrossRef
23.
go back to reference Sadick NS. A study to determine the efficacy of a novel handheld light-emitting diode device in the treatment of photoaged skin. J Cosmet Dermatol. 2008;7:263–7.CrossRef Sadick NS. A study to determine the efficacy of a novel handheld light-emitting diode device in the treatment of photoaged skin. J Cosmet Dermatol. 2008;7:263–7.CrossRef
24.
go back to reference Sadick NS. Handheld LED array device in the treatment of acne vulgaris. J Drugs Dermatol. 2008;7:347–50.PubMed Sadick NS. Handheld LED array device in the treatment of acne vulgaris. J Drugs Dermatol. 2008;7:347–50.PubMed
25.
go back to reference Spilker B. Guide to Clinical Trials. New York: Raven Press; 1991. Spilker B. Guide to Clinical Trials. New York: Raven Press; 1991.
26.
go back to reference Lev-Tov H, Mamalis A, Brody N, Siegel D, Jagdeo J. Inhibition of fibroblast proliferation in vitro using red light-emitting diodes. Dermatol Surg. 2013;39:1167–70.CrossRef Lev-Tov H, Mamalis A, Brody N, Siegel D, Jagdeo J. Inhibition of fibroblast proliferation in vitro using red light-emitting diodes. Dermatol Surg. 2013;39:1167–70.CrossRef
27.
go back to reference Le Tourneau C, Lee JJ, Siu LL. Dose escalation methods in phase I cancer clinical trials. J Natl Cancer Inst. 2009;101:708–20.CrossRef Le Tourneau C, Lee JJ, Siu LL. Dose escalation methods in phase I cancer clinical trials. J Natl Cancer Inst. 2009;101:708–20.CrossRef
28.
go back to reference Hanley JA, Lippman-Hand A. If nothing goes wrong, is everything all right? Interpreting zero numerators. JAMA. 1983;249:1743–5.CrossRef Hanley JA, Lippman-Hand A. If nothing goes wrong, is everything all right? Interpreting zero numerators. JAMA. 1983;249:1743–5.CrossRef
29.
go back to reference Anderson KL, Feldman SR. A guide to prescribing home phototherapy for patients with psoriasis: the appropriate patient, the type of unit, the treatment regimen, and the potential obstacles. J Am Acad Dermatol. 2015;72:868–78 e1.CrossRef Anderson KL, Feldman SR. A guide to prescribing home phototherapy for patients with psoriasis: the appropriate patient, the type of unit, the treatment regimen, and the potential obstacles. J Am Acad Dermatol. 2015;72:868–78 e1.CrossRef
30.
go back to reference Menter A, Korman NJ, Elmets CA, Feldman SR, Gelfand JM, Gordon KB, et al. Guidelines of care for the management of psoriasis and psoriatic arthritis: Section 5. Guidelines of care for the treatment of psoriasis with phototherapy and photochemotherapy. J Am Acad Dermatol. 2010;62:114–35.CrossRef Menter A, Korman NJ, Elmets CA, Feldman SR, Gelfand JM, Gordon KB, et al. Guidelines of care for the management of psoriasis and psoriatic arthritis: Section 5. Guidelines of care for the treatment of psoriasis with phototherapy and photochemotherapy. J Am Acad Dermatol. 2010;62:114–35.CrossRef
33.
go back to reference Travers JB, Spandau DF, Lewis DA, Machado C, Kingsley M, Mousdicas N, et al. Fibroblast senescence and squamous cell carcinoma: how wounding therapies could be protective. Dermatol Surg. 2013;39:967–73.CrossRef Travers JB, Spandau DF, Lewis DA, Machado C, Kingsley M, Mousdicas N, et al. Fibroblast senescence and squamous cell carcinoma: how wounding therapies could be protective. Dermatol Surg. 2013;39:967–73.CrossRef
34.
go back to reference Chaowattanapanit S, Silpa-Archa N, Kohli I, Lim HW, Hamzavi I. Postinflammatory hyperpigmentation: A comprehensive overview: Treatment options and prevention. J Am Acad Dermatol. 2017;77:607–21.CrossRef Chaowattanapanit S, Silpa-Archa N, Kohli I, Lim HW, Hamzavi I. Postinflammatory hyperpigmentation: A comprehensive overview: Treatment options and prevention. J Am Acad Dermatol. 2017;77:607–21.CrossRef
35.
go back to reference Gloster HM Jr, Neal K. Skin cancer in skin of color. J Am Acad Dermatol. 2006;55:741–60 quiz 761–4.CrossRef Gloster HM Jr, Neal K. Skin cancer in skin of color. J Am Acad Dermatol. 2006;55:741–60 quiz 761–4.CrossRef
36.
go back to reference Anderson RR, Parrish JA. Selective photothermolysis: precise microsurgery by selective absorption of pulsed radiation. Science. 1983;220:524–7.CrossRef Anderson RR, Parrish JA. Selective photothermolysis: precise microsurgery by selective absorption of pulsed radiation. Science. 1983;220:524–7.CrossRef
38.
go back to reference U.S. Department of Health and Human Services FDA Center for Drug Evaluation and Research, U.S. Department of Health and Human Services FDA Center for Biologics Evaluation and Research, U.S. Department of Health and Human Services FDA Center for Devices and Radiological Health. Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance. Health Qual Life Outcomes. 2006;4:79. U.S. Department of Health and Human Services FDA Center for Drug Evaluation and Research, U.S. Department of Health and Human Services FDA Center for Biologics Evaluation and Research, U.S. Department of Health and Human Services FDA Center for Devices and Radiological Health. Guidance for industry: patient-reported outcome measures: use in medical product development to support labeling claims: draft guidance. Health Qual Life Outcomes. 2006;4:79.
39.
go back to reference Baran R, Maibach HI, editors. Textbook of Cosmetic Dermatology. 5th ed. London: CRC Press; 2017. Baran R, Maibach HI, editors. Textbook of Cosmetic Dermatology. 5th ed. London: CRC Press; 2017.
40.
go back to reference Koehler MJ, König K, Elsner P, Bückle R, Kaatz M. In vivo assessment of human skin aging by multiphoton laser scanning tomography. Opt Lett. 2006;31:2879–81.CrossRef Koehler MJ, König K, Elsner P, Bückle R, Kaatz M. In vivo assessment of human skin aging by multiphoton laser scanning tomography. Opt Lett. 2006;31:2879–81.CrossRef
Metadata
Title
A single-blind, dose-escalation, phase I study of high-fluence light-emitting diode-red light on Caucasian non-Hispanic skin: study protocol for a randomized controlled trial
Authors
Erica B. Wang
Ramanjot Kaur
Julie Nguyen
Derek Ho
Evan Austin
Emanual Maverakis
Chin-Shang Li
Samuel T. Hwang
R. Rivkah Isseroff
Jared Jagdeo
Publication date
01-12-2019
Publisher
BioMed Central
Keyword
Phototherapy
Published in
Trials / Issue 1/2019
Electronic ISSN: 1745-6215
DOI
https://doi.org/10.1186/s13063-019-3278-7

Other articles of this Issue 1/2019

Trials 1/2019 Go to the issue