Phase IV, Randomized, Double-blind Study on Muscle Activity of Two Commercial Preparations of Botulinum Toxin Type A (Dysport and Xeomin) Administered to the Upper Third of the Face (Forehead Lines).
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Percentage of Responders After 5 Months After the Procedure
研究概览
简要总结
this study was proposed to provide more scientific and objective data on the clinical and aesthetic effects of these two toxins (Dysport and Xeomin).
详细描述
Subjects will perform 6 (six) visits during the study:
Screening visit, performed 30 to 1 day before the visit 1, when eligible subjects will be recruited and first evaluations will be performed; visit 1, which is the baseline and when the injections will be performed; visit 2, 30 +/- 3 days after the injections, when evaluations will be performed; visit 3, 90 +/- 3 days after the injections, when evaluations will be performed; 4, 120 +/- 3 days after the injections, when evaluations will be performed; visit 5, 150 +/- 3 days after the injections, when evaluations will be performed.
Assessment of percentage (%) of responders, after 5 months of injection, to the effects of two BT-A preparations, Dysport® and Xeomin®, by measuring frontalis m. wrinkle intensity at maximum contraction, as measured by visual Wrinkles Severity Scale (WSS).
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Subject agreement to provide written informed consent and the willingness and ability to comply with all aspects of the protocol;
- •Female subjects;
- •Phototype I to IV;
- •Subjects aged between 18 and 60 years;
- •Subjects naive for BT-A treatment;
- •Subjects presenting the same degree of moderate (2) to severe (3) wrinkles on the left and right side of forehead under maximum voluntary contraction of the frontalis m. according WSS;
- •Subjects with Minor's test showing at least grade III in the Sweating Intensity Visual Scale;
- •Medical history and physical examination which, based on the investigator's opinion, do not prevent the subject from taking part in the study or from making use of the products under investigation;
- •Subjects of childbearing age should present a negative urine pregnancy test at baseline and should be using a highly effective contraceptive method during all study;
- •Availability of the subject throughout the study (5 months);
- •Subject agreeing not to undergo other cosmetic or dermatological procedures during the participation in the study;
- •Subjects with sufficient schooling and knowledge to enable them to cooperate to the degree required by the protocol.
排除标准
- •Pregnant women or women intending to become pregnant in the following 5 months after screening;
- •Lactation period;
- •Subjects participating in other clinical trials;
- •Any prior surgery affecting the frontalis and/or orbicularis muscles, prior blepharoplasty or brow lift;
- •Any prior cosmetic procedures, including fillers, or scars that may interfere with the study results;
- •Subjects with neoplastic, muscular or neurological diseases;
- •Subjects taking aminoglycoside and penicillamine antibiotics, quinine or Ca2+ channel blockers;
- •Subjects with inflammation or active infection in the area to be injected;
- •Subjects presenting evident facial asymmetry;
- •Subjects with a history of adverse effects, such as sensitivity to the components of any of the study drug formula, ptosis or any other adverse effect which, in the investigator's opinion, should prevent the subject from participating in the study;
- •Subjects presenting Myasthenia Gravis, Eaton-Lambert Syndrome and motor neuron disease;
- •Subjects with coagulation disorders or taking anticoagulants;
- •Subjects with known systemic autoimmune diseases;
- •Subjects with a history of non-adherence to medical treatment or showing unwillingness to adhere to the study protocol;
- •Any condition that, in the opinion of the investigator, can compromise the evaluation of the study.
研究组 & 干预措施
Dysport and Xeomin
30 U of Dysport® was injected on the right side of the forehead and 12 U Xeomin® was injected on the left side of the forehead (dose-equivalence 2.5:1).
干预措施: Dysport (Drug)
Dysport and Xeomin
30 U of Dysport® was injected on the right side of the forehead and 12 U Xeomin® was injected on the left side of the forehead (dose-equivalence 2.5:1).
干预措施: Xeomin (Drug)
Xeomin and Dysport
30 U Dysport® was injected on the left side of the forehead and 12 U Xeomin® was injected on the right side of the forehead (dose-equivalence 2.5:1).
干预措施: Dysport (Drug)
Xeomin and Dysport
30 U Dysport® was injected on the left side of the forehead and 12 U Xeomin® was injected on the right side of the forehead (dose-equivalence 2.5:1).
干预措施: Xeomin (Drug)
结局指标
主要结局
Percentage of Responders After 5 Months After the Procedure
时间窗: 5 months after intervention
Percentage (%) of responders, after 5 months of injection, to the effects of two botulinum toxin type A (BT-A), Dysport® and Xeomin®. Responders were defined as individuals who presented at least 1 score less in the Wrinkles Scale Score (WSS) at maximum contraction compared to the WSS score at baseline. WSS is a validated 4-point scale, at rest and at maximum voluntary contraction of the frontalis muscle, in which 0 means no wrinkles up to 3 which means sever wrinkles.
次要结局
- Maximum Evoked Compound Muscle Action Potential(5 months after the procedure.)
研究者
Doris Hexsel
MD
Brazilan Center for Studies in Dermatology