A Single Center, Prospective, Open-label, Clinical Trial Using Micro-injections of Transparent Hyaluronic Acid Gel (Restylane® Silk) for Rejuvenation of the Aging Cheek
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 20
- 试验地点
- 2
- 主要终点
- Hydrometer measured Transepidermal Water Loss
研究概览
简要总结
The objective of this study is to determine the efficacy and safety of Restylane® Silk microinjections when used in a grid-like injection pattern for the correction of fine lines to the cheeks.
详细描述
Silk for correction of mid to low cheek fine lines and wrinkles. Twenty (20) subjects will be enrolled. Each subject will receive Restylane® Silk to the entire cheeks. The defined area will be defined as the following: line extending from the upper margin of the nasal ala to the upper margin of the tragus, from the tragus to 1 cm above the mandibular angle, from 1 cm above the mandibular angle to 1 cm above the pre-jowl sulcus, and from 1 cm above the pre-jowl sulcus to the upper margin of the nasal ala. The injections will be delivered intradermally via multiple 0.02 cc microinjections distributed in a grid array pattern with 1-2 cm between each injection point (see figure 1; injections will extend 1 cm above the illustration). Following completion of injection treatment, manual massage will be applied to the full area to promote even distribution of the product. Each subject will undergo a total of three treatment sessions, one month apart, day 1, week 4, and week 8. The maximum amount of Restylane to be used per treatments session/per cheek is 1.5cc (not to exceed a total of 9 cc) per treated patient. Three-dimensional digital photography utilizing the Vectra 3D System (Canfield) will be utilized to document pre-treatment status, sites of injection, and post-treatment effect. Subjects will be followed up at 4 weeks, 8 weeks, post-treatment day 90, and day 180. Objective measures of efficacy will be me performed pre-treatment, at day 90 and 180.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •b. Symmetrical visible sign of aging involving at least a 9 cm2 area of the mid to low cheeks.
- •c. Must be willing to give and sign a HIPPA form, photo consent and informed consent form.
- •d. Must be willing to comply with study dosing and complete the entire course of the study.
- •e. Female patients will be either of non-childbearing potential defined as:
- •Having no uterus
- •No menses for at least 12 months. Or; (WOCBP) women of childbearing potential must agree to use an effective method of birth control during the course of the study, such as:
- •Oral contraceptive pill, injection, implant, patch, vaginal ring, intrauterine device
- •Intrauterine coil
- •Bilateral tubal ligation
- •Barrier method used with an additional form of contraception (e.g., sponge, spermicide or condom)
- •Abstinence (If practicing abstinence must agree to use barrier method described above (4) if becomes sexually active).
- •Vasectomized partner (must agree to use barrier method described above (4) if becomes sexually active with un-vasectomized).
- •f. Negative urine pregnancy test results Baseline prior to study entry (if applicable)
排除标准
- •Pregnant, planning pregnancy during the course of the study or breastfeeding
- •Extremely Severe aging face with extensive photodamage
- •Previous use of any form of soft tissue augmentation in the treatment area within the past 12 months
- •Pre-existing medical or dermatologic condition in the treatment area that may affect the treatment or interpretation of treatment effect (at investigator discretion)
- •Presence of tattoo and/or scar in the treatment area that in the investigators opinion would interfere with study assessments
- •Use of oral/topical retinoids within 1 month of Baseline
- •Previous use of botulinum toxins in the treatment area within the past 6 months
- •Previous surgical procedure in the treatment area within the past 12 months
- •Presence or evidence of any conditions that in the opinion of the investigator might impede the subject's ability to give consent or comply with protocol requirements.
- •Current participation or participation within 30 days prior to the start of this study in a drug or other investigational research study
- •History of non-compliance with clinical research protocols
- •Ablative laser resurfacing to on their face within 12 months
- •Non-ablative laser or light procedures to their face within the past 3 months
- •Known allergy to Restylane® Silk or any of its constituents
研究组 & 干预措施
Hyaluronic Acid Microinjection
干预措施: Restylane® Silk (Device)
结局指标
主要结局
Hydrometer measured Transepidermal Water Loss
时间窗: Baseline to 6 - Months Post Final Treatment
Change in transepidermal waterloss from baseline to the last visit measured using a hydrometer.
Investigator five point global aesthetic improvement score
时间窗: Baseline to 6 - Months Post Final Treatment
Change in Investigator five point global aesthetic improvement score from Baseline at all follow up visits through month 6 using Investogator's Global Aesthetic Improvement Scale
Cutometer Measured Skin Elaticity
时间窗: Baseline to 6 - Months Post Final Treatment
Change in elasticity from baseline to the last visit measured using a Cutometer
次要结局
- Safety - Injection Site Adverse Events(Baseline to 6 - Months Post Final Treatment)
研究者
Isabella Guiha
Certified Clinical Research Coordinator
Dermatology Cosmetic Laser Medical Associates of La Jolla, Inc.