Pilot Study of a Novel IPL for Removal of Unwanted Fine Body Hair

NCT ID: NCT01912950

Last Updated: 2023-02-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 11 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-12-31
• Study Completion Date: 2015-07-31

Brief Summary

The purpose of this randomized, controlled, open-label pilot study is to evaluate the safety and efficacy of a novel intense pulsed light (IPL) device for removal of unwanted fine body hair.

Subjects will have IPL treatment on one forearm area. Another area will serve as the un-treated control area. Subjects will be followed at 12-weeks post-final treatment.

Conditions

Hypertrichosis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Prowave LX IPL

One area on forearm will receive treatment with Prowave LX IPL

Group Type: EXPERIMENTAL

Prowave LX IPL

Intervention Type: DEVICE

No Treatment

No treatment administered on one area of forearm

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Prowave LX IPL

Intervention Type: DEVICE

Other Intervention Names

Prowave; Prowave LX; Cutera Prowave LX; Intense Pulsed Light; IPL; Flashlamp Infared device; Hair removal

Eligibility Criteria

Inclusion Criteria

• Female or Male, 18 to 65 years of age (inclusive).
• Fitzpatrick Skin Type I - III.
• Subject has black or dark brown unwanted arm hair of fine texture.
• Willing to have the hair removal procedure on one forearm only, and within the designated study treatment area.
• Willing and able to adhere to the treatment and follow-up schedule, and the study "Before and After Procedure Instructions".
• Willing to refrain from shaving the treatment area for 5 days prior to each study visit.
• Must be able to read, understand and sign the Informed Consent Form.
• Must agree not to use hair removal products, such as topical chemical depilatories, or undergo any other hair removal procedure during the study, such as other laser and light therapies or waxing.
• Willing to refrain from excess sun exposure and willing to wear sunscreen on the treatment area during the study (including the follow-up period).
• Willing to have digital photographs taken of the treatment area and agree to use of photographs for presentation, educational or marketing purposes.
• Must be in good health, as determined by the Investigator.
• Must be post-menopausal or surgically sterilized, or using a medically acceptable form of birth control at least 3 months prior to enrollment and during the entire course of the study.

Exclusion Criteria

• Participation in a clinical trial of another device or drug within 6 months prior to enrollment, or during the study.
• Had any type of professional hair removal procedure, such as laser, light-based, RF or electrolysis, in the treatment area within 12 months of study participation.
• Had other epilation treatment, such as waxing or mechanical epilator, in the treatment area within 6 months of study participation.
• Subject shows signs of actinic bronzing or recent tanning in the treatment area, and unable/unlikely to refrain from tanning during the study.
• Subject is pregnant and/or breastfeeding.
• Suffering from significant concurrent illness, such as diabetes mellitus or pertinent neurological disorders.
• Having malignant or pre-malignant lesions in the treatment area, or history of a malignant skin disease.
• Current acute or chronic skin infections or inflammatory processes, affecting the treatment area, such as dermatitis.
• Currently using immunosuppressive medications or history of immunosuppression/immune deficiency disorder, such as psoriasis, eczema, vitiligo, systemic lupus erythematosus or scleroderma.
• Current use of any medication that is known to increase sensitivity to light, such as tetracycline.
• Currently undergoing systemic chemotherapy or radiation treatment for cancer, or history of treatment within 3 months of study participation.
• Suffering from coagulation disorders or taking prescription anticoagulation medications.
• History of keloid formation, hypertrophic scarring or abnormal/delayed wound healing.
• History of seizure disorders due to light.
• History of diseases stimulated by heat, such as recurrent herpes zoster in the treatment area, unless treatment is conducted following a prophylactic regimen.
• History of pigmentary disorders, particularly tendency for hyper- or hypo-pigmentation.
• History of tattoo, permanent make-up or semi-permanent or permanent tissue fillers in the treatment area.
• Systemic use of a retinoid (such as Accutane) or corticosteroid within 6 months of study participation.
• Current smoker or history of smoking within 12 months of study participation.
• Anytime in life, had used gold therapy (gold salts) for disorders such as rheumatologic disease or lupus.
• As per the Investigator's discretion, any physical or mental condition which might make it unsafe for the subject to participate in this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Cutera Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Neil Sadick

Role: PRINCIPAL_INVESTIGATOR

Study Principal Investigator

Locations

Sadick Research Group

New York, New York, United States

Countries

United States

Other Identifiers

C-13-PW01

Identifier Type: -

Identifier Source: org_study_id