Histological Study of the Effects of a 2910 nm Fiber Laser Technology
Launched by FA CORPORATION · Mar 12, 2024
Trial Information
Current as of July 23, 2025
Enrolling by invitation
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Healthy male and female adults between 18-75 years of age.
- • Subjects who can read, understand, and sign the Informed Consent Form.
- • Subjects willing and able to comply with all study requirements.
- • Fitzpatrick skin types I-IV.
- • Subjects who have pre-scheduled a body or facial contouring procedure.
- Exclusion Criteria:
- • Subjects with active localized or systemic infections
- • Immunocompromised subjects
- • Subjects with coagulation disorder
- • History of radiation therapy to treatment area
- • Subject with a history of lidocaine or ester-based local anesthetics
- • Pacemaker or internal defibrillator
- • Superficial or metal implants in the area
- • Current or history of skin cancer, as well as any other type of cancer, or pre-malignant moles.
- • Severe concurrent conditions, such as cardiac disorders
- • Pregnancy and nursing
- • Impaired immune system due to immunosuppressive diseases such as AIDS and HIV, or use of immunosuppressive medications.
- • Diseases which may be stimulated by light at the wavelengths used, such as history of Systemic Lupus Erythematosus, Porphyria, and Epilepsy.
- • Patients with a history of diseases stimulated by heat, such as recurrent Herpes Simplex in the treatment area, may be treated only following a prophylactic regime.
- • Any active condition in the treatment area, such as sores, psoriasis eczema, and rash.
- • History of skin disorders, keloids, abnormal wound healing, as well as very dry and fragile skin.
- • History of bleeding coagulopathies or use of anticoagulants.
- • Use of medication and herbs known to induce photosensitivity to light exposure at the wavelengths used, such as Isotretinoin (Accutane) within the last 6 months, tetracyclines, or St. John's Wort within the last two weeks.
- • Any surgical procedure in the treatment area within the last 3 months or before complete healing.
- • Tattoo or permanent makeup in the treatment area.
- • Excessively tanned skin from sun, tanning beds or tanning creams within last the two weeks.
- • As per the practitioner's discretion, refrain from treating any condition which might make it unsafe for the patient
About Fa Corporation
FA Corporation is a leading clinical trial sponsor dedicated to advancing medical research and innovation. With a strong focus on therapeutic areas such as oncology, neurology, and rare diseases, FA Corporation leverages cutting-edge methodologies and a robust network of research sites to facilitate efficient and effective clinical studies. Committed to upholding the highest standards of regulatory compliance and ethical considerations, FA Corporation collaborates closely with healthcare professionals and regulatory bodies to ensure the safety and well-being of trial participants. Through its strategic partnerships and commitment to scientific excellence, FA Corporation strives to bring transformative therapies to market, ultimately improving patient outcomes and enhancing the quality of life.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Dallas, Texas, United States
Patients applied
Trial Officials
Shlomo Assa, President FACorp
Study Director
FA Corporation
Jeffrey Kenkel, MD
Principal Investigator
UT Southwestern Medical Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported