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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02492373
Other study ID # Si 033/2015
Secondary ID
Status Completed
Phase N/A
First received June 27, 2015
Last updated May 31, 2016
Start date February 2015
Est. completion date May 2016

Study information

Verified date May 2016
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Interventional

Clinical Trial Summary

To investigate the benefit of the application of topical high potency steroid on the incidence of post inflammatory hyperpigmentation after laser treatment.


Description:

- The incidence of post inflammatory hyperpigmentation (PIH) after treating lentigines with Q-switched Nd:YAG laser was 78.3%.

- It has been found that the incidence of PIH decreased to 40% after applied topical high potency steroid 2 days after the laser treatment.

- By these anti-inflammatory and anti-PIH effects of the high potency steroid, the investigators aimed that the application of steroid 2 days before and 2 days after the laser treatment would be better reduction in the incidence of PIH after Q-switched Nd:YAG laser.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Having multiple lentigines on both sides of the face

- Fitzpatrick skin phototype 3-5

Exclusion Criteria:

- Patients with lesions with any clinical suspicion of being pre-cancerous or skin malignancies of any kind

- Patients who have photosensitive dermatoses

- Pregnancy and lactation woman

- Patients with wound infections (herpes, other) on the day of treatment

- Patients with moderate and severe inflammatory acne, Immunosuppressed patients, history of vitiligo

- Patients with unrealistic concerns/expectations and inability to do the appropriate post-operative care

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
topical 0.05% Clobetasol propionate ointment
Apply only on the treated area twice a day as mentions
Device:
Q switched Nd:YAG laser 532 nm
Treatment of facial lentigines. The energy using depends on the endpoint of immediate whitening of the lesions.

Locations

Country Name City State
Thailand Faculty of Medicine Siriraj Hospital, Mahidol University Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

References & Publications (4)

Cheyasak N, Manuskiatti W, Maneeprasopchoke P, Wanitphakdeedecha R. Topical corticosteroids minimise the risk of postinflammatory hyper-pigmentation after ablative fractional CO2 laser resurfacing in Asians. Acta Derm Venereol. 2015 Feb;95(2):201-5. doi: — View Citation

Ho SG, Yeung CK, Chan NP, Shek SY, Chan HH. A comparison of Q-switched and long-pulsed alexandrite laser for the treatment of freckles and lentigines in oriental patients. Lasers Surg Med. 2011 Feb;43(2):108-13. doi: 10.1002/lsm.21045. — View Citation

Jun HJ, Cho SH, Lee JD, Kim HS. A split-face, evaluator-blind randomized study on the early effects of Q-switched Nd:YAG laser plus Er:YAG micropeel (combined therapy) versus Q-switched Nd:YAG alone in light solar lentigines in Asians. Lasers Med Sci. 201 — View Citation

Takiwaki H, Shirai S, Kohno H, Soh H, Arase S. The degrees of UVB-induced erythema and pigmentation correlate linearly and are reduced in a parallel manner by topical anti-inflammatory agents. J Invest Dermatol. 1994 Nov;103(5):642-6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The incidence of post inflammatory hyperpigmentation By investigator's observation. 2 weeks Yes
Secondary Side effects of topical steroid By investigators' observation of telangiectasia, erythema or atrophy. Follow-up 2, 3, 4, 8, 12 and 24 weeks after the last treatment Yes
Secondary The patients satisfaction By using Quartile grading scale of improvement; 0 = not improve, 1= 1-25% improvement, 2 = 26-50% improvement, 3 = 51-75% improvement and 4 = 76-100% improvement Follow-up 4, 8, 12 and 24 weeks after the last treatment Yes
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Not yet recruiting NCT06305897 - Evaluation of the Tolerance (Main Objective) and Performance of Cyto-selective Difluoroethane-based Cryotherapy in the Treatment of Brown Spots (Solar and Senile Lentigines, Post-inflammatory Hyperpigmentation) on the Face N/A
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