Clinical Study to Evaluate the Safety and Effectiveness of the Treatment With Tixel C on Acne Scars

A Prospective Study With Blinded Assessment to Evaluate the Safety and Effectiveness of the Tixel C Fractional System in the Treatment of Acne Scars

The purpose of this research is to evaluate the safety and effectiveness of the Tixel C device for the treatment of acne scars, for improvement in the appearance of surface texture.

Study Overview

• Status: Withdrawn
• Conditions: Scars
• Intervention / Treatment: Device: Tixel C

Detailed Description

44 participents between two research locations with moderate acne scars will receive 3-5 treatments sessions with the Tixel C device according to investigator's review of subject response. Improvement of acne scarring will ve evaluated at 1 month, 3 months and 6 months post treatment.

Post-treatment response will be evaluated as well as any incidence of side efects throughout the study.

• Study Type: Interventional
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Israel
  • Herzliya, Israel, 4672553
    • The Lehavit Akerman Main Clinic
• United States
  • Illinois
    • Chicago, Illinois, United States, 60611
      • Physicians Laser and Dermatology Institute

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. The Subjects will have atrophic mild to severe acne scars.
2. Male or female subjects, age 18-65 years old.
3. The subjects will have Fitzpatrick Skin Types I-VI.
4. Willingness and ability to provide written informed consent, including photo consent and adherence to photography procedures (i.e., removal of jewelry and makeup), prior to the study.
5. Willingness and ability to comply with protocol requirements, including returning for follow-up visits and abstaining from exclusionary procedures for the duration of the study.
6. Females 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 (i.e., oral contraceptives, IUD, contraceptive implant, barrier methods with spermicide, or abstinence).

Exclusion Criteria:

1. Subjects pregnant or planning to become pregnant, or have given birth less than three months ago or breast feeding.
2. Subjects with significant exposure to ultraviolet light.
3. Use of drugs that may induce hyperpigmentation such as amiodarone, clofazinmine, minocycline or chloroquine.
4. History of facial acne scar treatments with laser, surgical, chemical, light based or radiofrequency facial treatments.
5. Microdermabrasion, or prescription level glycolic acid treatments within three months prior to study participation.
6. Active HSV-1. May be enrolled only after a prophylactic regime has been followed prior to treatment and according to the Investigator's discretion.
7. History of keloid formation.
8. Permanent facial implant over area of treatment.
9. Injectable filler in area to be treated within nine months of investigation.
10. History of collagen vascular disease.
11. Subjects who have an impaired immune system, suffer from immunosuppressive diseases or are actively on immunosuppressive medications.
12. Subjects currently taking or have taken an oral retinoid in the past six months.
13. Subjects currently taking long-term oral steroid treatment
14. Subjects with any skin pathology which can induce bullous lesions, urticaria, or demonstrate a Koebner phenomenon (psoriasis, lichen planus, etc.).
15. History of autoimmune disease.
16. History of any disease that inhibits pain sensation.
17. History of Diabetes I or II.
18. Concurrent therapy that, in the principal investigator's opinion, would interfere with the evaluation of the safety or effectiveness of the study treatment.
19. Subjects who, in the Investigator's opinion, have a history of poor cooperation, non-compliance with medical treatment or unreliability.
20. Enrollment in any active study involving the use of investigational devices or drugs who in the Investigator's opinion would interfere with the evaluation of the current investigative device.
21. Any other contraindication stated in the guidance documents of the treatment device.
22. Any existing skin disease that in the investigator's opinion would interfere with the evaluation of the safety of the study treatment and any other cause per the principal investigator's discretion.
23. Hypertrophic facial acne scarring or other hypertrophic scarring.
24. Failure to acquire adequate baseline and final photography.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Tixel C; Tixel Treatment, between 3-5 treatment session according to investigator's review of subject response follow by 3 Follow up sessions, 1,3 and 6 month after last treatment visit. Subject would be questioned about pain levvel, subjective dountime assessment and subjective response assessment. Images would be taken before treatment visit and in Follow-Up.	Device: Tixel C; Thermo-mechanical technology for fractional treatment of human skin. Dermal heating and coagulative effect that occur during the treatment session provide for dermal remodeling and collagen restructuring that promote acne scar appearance improvement.; Other Names: Fractional

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Safety Adverse Events report	Safety of the investigational device shall be assessed via quantification of the incidence of devicerelated/non-related undesired effects, which shall be documented and reported as an Adverse Event (AE) or as a Serious Adverse Event (SAE). Known undesired effects may be any of the list stated in the previous paragraph of Expected Possible Side Effects, or any other undesired effect, not described in the said list. The incidence of the device related undesired effects should be analyzed considering severity, causal relation to the investigational device and duration, whether it is transient or permanent.	up to 12 months
Effectiveness using Goodman and Baron Assessment scale	Before starting therapy and at one and six months follow up visits, the subjects shall be photographed using clinical photography equipment. The images shall be evaluated by blinded raters. The evaluation shall be performed by three raters. The scores shall be analyzed according to the statistical plan of the study. Scale between 1-4; 1 = Macular, 4= Severe	up to 12 months; Improvement between last follow up and baseline (before first treatment)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Performance using Goodman and Baron Assessment scale	Live Assessment by a study investigator - In each visit, an investigator or his designee shall examine by observing the subject and photographs will be taken as outlined. Scale between 1-4; 1 = Macular, 4= Severe	up to 12 months; Improvement between last follow up and baseline (before first treatment)

Collaborators and Investigators

• Sponsor: Novoxel Ltd.

Study record dates

Study Major Dates

• Study Start (Anticipated): March 1, 2020
• Primary Completion (Actual): January 10, 2021
• Study Completion (Actual): January 10, 2021

Study Registration Dates

• First Submitted: February 6, 2020
• First Submitted That Met QC Criteria: February 12, 2020
• First Posted (Actual): February 13, 2020

Study Record Updates

• Last Update Posted (Actual): January 12, 2021
• Last Update Submitted That Met QC Criteria: January 10, 2021
• Last Verified: January 1, 2021

More Information

Terms related to this study

• Keywords: Scars; Acne Scars; Post Acne
• Additional Relevant MeSH Terms: Pathologic Processes; Fibrosis; Cicatrix
• Other Study ID Numbers: CLN 0472

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: Yes
• product manufactured in and exported from the U.S.: No