Injectable Poly-L-Lactic Acid for Volumization and Adipogenesis of the Hip Dell

Skin Laxity Clinical Trial

Official title:

A Single Center, Double-Blinded, Split-Body, Randomized Clinical Trial of Injectable Poly-L-Lactic Acid for Volumization and Adipogenesis of the Hip Dell

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05269654
• Other study ID #: Sculptra Aesthetic - Hip Dell
• Status: Not yet recruiting
• Phase: N/A
• Start date: March 4, 2022
• Est. completion date: March 1, 2024

Study information

• Verified date: February 2022
• Source: Goldman, Butterwick, Fitzpatrick and Groff
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To assess the safety, efficacy and subject satisfaction associated with volumization of the hip dell with injectable poly-L-lactic acid (PLLA), or Sculptra® Aesthetic (Galderma Laboratories, Fort Worth, TX).

Description:

The primary objectives of this clinical trial is to assess efficacy of adipose tissue generation (adipogenesis) and volumization following treatment of the hip dell with injectable poly-L-lactic acid (PLLA, Sculptra® Aesthetic; Galderma Laboratories; Fort Worth, TX). Enrolled subjects will be randomized to two (2) treatment groups: "right hip dell treated" and "left hip dell treated". All subjects will receive three (3), single-sided injections of Sculptra® Aesthetic (Galderma Laboratories; Fort Worth, TX), performed one (1) month ± 7 days apart. Treatments will be provided to one side randomly assigned to either "right side" or "left side". The non-treatment side will receive bacteriostatic saline, injected in the same manner as Sculptra® Aesthetic. One (1) vial of Sculptra® Aesthetic, diluted to 8mL, will be used per treatment session. Subjects satisfying all inclusion and no exclusion criteria will be enrolled in this trial. Prior to receiving any study treatment, mandatory digital photography with overhead lighting and VECTRA® (Canfield Scientific, Inc.; Parsippany, NJ) 3D volumetric body photography will be obtained of each subject's treatment area. In order to participate in the study, subjects must provide written informed consent to have their photographs used for research, publication, and/or commercial purposes.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: March 1, 2024
• Est. primary completion date: December 31, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 30 Years to 60 Years

Eligibility

Inclusion Criteria:

• Adult females aged 30 to 60 years
• Subjects in good general health based on investigator's judgment and medical history
• Moderate to severe hip dell volume deficit as determined by the investigators
• Must be willing to give and sign an informed consent form and photographic release form
• Must have a stable body weight for at least six (6) months prior to study entry
• Must be willing to maintain usual sun exposure, diet, and exercise routines for the duration of the study
• Subject agrees to avoid tanning or use of sunless tanner during the entire course of the study
• Negative urine pregnancy test result at the time of study entry (if applicable)
• For female subjects of childbearing potential, must be willing to use an acceptable form of birth control during the entire course of the study. All systemic birth control measures must be in consistent use for at least 30 days prior to study enrollment.
• A female is considered of childbearing potential unless she is postmenopausal, without a uterus and/or both ovaries, or has had a bilateral tubal ligation.
• Acceptable methods of birth control are: oral contraceptives, contraceptive patches/rings/implants, Implanon®, Depo-Provera®, double-barrier methods (e.g., condoms and spermicide), abstinence, and/or vasectomy of partner with a documented second acceptable method of birth control, should the subject become sexually active.
• Must be willing to comply with study treatments and complete the entire course of the study

Exclusion Criteria:

• Liposuction to bilateral hips, flanks, thighs, buttocks during the 12-month period prior to study treatment or any time during the course of the study
• Mesotherapy, dermal fillers, biostimulatory injectables, fat grafting, radiofrequency device treatments, microfocused ultrasound device treatments, laser and light-based device treatments, microneedling, cryolipolysis, high intensity focused electromagnetic energy device treatment, or surgery (i.e., lower body lift, buttocks augmentation, abdominoplasty, etc.) during the 12-month period before study treatment c) Any investigational treatment for a volume deficit of the bilateral hip dell areas during the 12-month period before the study treatment d) Massage therapy during the 3-month period before study treatment. e) Creams/cosmeceuticals and/or home therapies to promote plumping of the bilateral hip dell area during the four-week period before study treatment f) Subjects with scarring in the treatment areas g) History of thrombosis, post-thrombosis syndrome, or any vascular disorder of the bilateral lower extremities
• Any history of bleeding or coagulation disorders i) Subjects with tattoos or permanent implants in the treatment areas j) Subjects with a significant history or current evidence of a medical, psychological, or other disorder that, in the investigator's opinion, would preclude enrollment into the study
• Subjects with a history of or presence of any skin condition/disease (including but not limited to any visible rash, atopic dermatitis, psoriasis, actinic keratoses, keratinocyte carcinoma, melanoma, etc.) in the treatment area that might interfere with the diagnosis or evaluation of study parameters
• History of keloid or hypertrophic scarring
• Subjects with an active bacterial, viral, or fungal infection of the treatment areas
• Subjects who spray tanned or used sunless tanners in the treatment areas four (4) weeks prior to study treatment
• History of lidocaine sensitivity deemed by the investigator to preclude the subject from enrolling into the study
• Subjects planning any cosmetic procedure to the treatment areas during the study period, other than the treatment that will be performed by the investigator
• Presence of incompletely healed wound(s) in the treatment area
• Subjects who are on an immunosuppressant or have an autoimmune condition
• Female subjects who are pregnant, planning a pregnancy, or breast feeding during the study
• Current participation or participation within 30 days prior to the start of this study in a drug or other investigational research study

Related Conditions & MeSH terms

• Cutis Laxa
• Skin Laxity

Intervention

Device:
• injectable poly-L-lactic acid
Injectable biostimulant for volume loss

Other:
• Normal Saline
Sham Comparator

Locations

Country	Name	City	State
United States	West Dermatology Research Center/Cosmetic Laser Dermatology	San Diego	California

Sponsors (2)

Lead Sponsor	Collaborator
Goldman, Butterwick, Fitzpatrick and Groff	Galderma R&D

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Histological Analysis	Comparison of measure of adipose tissue in biopsies taken from device and sham treated areas prior to baseline and at followup visits	Baseline to three months post final treatment
Primary	Histological Analysis	Comparison of measure of adipose tissue in biopsies taken from device and sham treated areas prior to baseline and at followup visits	Baseline to six months post final treatment
Primary	Volumetric Analysis	Analysis of tissue volume in treatment zones based on measurements obtained via 3D photography	Pre-Treatment Visit 2/ Baseline
Primary	Volumetric Analysis	Analysis of tissue volume in treatment zones based on measurements obtained via 3D photography	Pre-Treatment Visit 3/ Day 14
Primary	Volumetric Analysis	Analysis of tissue volume in treatment zones based on measurements obtained via 3D photography	Pre-Treatment Visit 4/ Day 44
Primary	Volumetric Analysis	Analysis of tissue volume in treatment zones based on measurements obtained via 3D photography	Pre-Treatment Visit 5/ Day 74
Primary	Volumetric Analysis	Analysis of tissue volume in treatment zones based on measurements obtained via 3D photography	Visit 6/ Day 104
Primary	Volumetric Analysis	Analysis of tissue volume in treatment zones based on measurements obtained via 3D photography	Visit 7/ Day 164
Primary	Volumetric Analysis	Analysis of tissue volume in treatment zones based on measurements obtained via 3D photography	Visit 9/ Day 254
Primary	Volumetric Analysis	Analysis of tissue volume in treatment zones based on measurements obtained via 3D photography	Visit 11/ Day 344
Primary	Physician Global Aesthetic Improvement Scale	Blinded-Evaluator assessment of change in appearance of treated areas where 1 + Very Much Improved, 2 = Much Improved, 3 = Improved, 4 = No Change, and 5 = Worse	1 Month Follow-Up visit
Primary	Physician Global Aesthetic Improvement Scale	Blinded-Evaluator assessment of change in appearance of treated areas where 1 + Very Much Improved, 2 = Much Improved, 3 = Improved, 4 = No Change, and 5 = Worse	3 Month Follow-Up visit
Primary	Physician Global Aesthetic Improvement Scale	Blinded-Evaluator assessment of change in appearance of treated areas where 1 + Very Much Improved, 2 = Much Improved, 3 = Improved, 4 = No Change, and 5 = Worse	6 Month Follow-Up visit
Primary	Physician Global Aesthetic Improvement Scale	Blinded-Evaluator assessment of change in appearance of treated areas where 1 + Very Much Improved, 2 = Much Improved, 3 = Improved, 4 = No Change, and 5 = Worse	9 Month Follow-Up visit
Primary	Identification of correct Treatment Area (Right vs Left Hip)	Blinded-Evaluator performed assessment of which side received study treatment and which received sham	9 Month Follow-Up visit
Secondary	Collagen Analysis	Quantitative analysis of collagen amounts based on histology	Upon analysis of biopsies collected at Day 0 and 3 and 6 Month Follow-Up visits
Secondary	Elastin Analysis	Quantitative analysis of elastin amounts based on histology	Upon analysis of biopsies collected at Day 0 and 3 and 6 Month Follow-Up visits
Secondary	Skin Thickness	Ultrasound imaging measurements of skin thickness/thickness of dermis	Day 0 and 3, 6, and 9 Month Follow-Up visits
Secondary	Subject Global Aesthetic Improvement Score	Subject assessment of change in appearance of treated areas rated numerically from 1 to 5 with 1 being very much improved to 5 being worse	1, 3, 6, and 9 Month Follow-Up visits
Secondary	Subject Satisfaction Questionairre	Degree of subject satisfaction with treatment outcomes rated numerically from 0 to 4 with 0 being not satisfied to 4 being extremely satisfied	1, 3, 6, and 9 Month Follow-Up visits
Secondary	Evaluation of Side Effects	Assessment of treatment related adverse events by Investigator	Day 44, Day 74, Day 104, Day 164, Day 178, Day 254, Day 268, Day 433