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临床试验/NCT03836638
NCT03836638Unknown不适用

The Impact of Age on Botulinum Toxin Potency in Facial Rhytides Treatment: A Prospective Randomized Controlled Trial

St Joseph University, Beirut, Lebanon1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2019年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
45
试验地点
1
主要终点
Changes of scores of Validated photonumeric scales: Brow Positioning Scale at rest

研究概览

简要总结

Botulinum toxin is approved by the FDA for the treatment of facial wrinkles. Patients are usually older than 45 years and their main demand is to treat pre-existing facial wrinkles. However with the increasing popularity of this technique, younger patients, aged 25 to 35 years, are now seeking botulinum toxin injection as a preventive measure for rhytides. The usual dose used for the treatment of facial rhytides in a female patient older than 45 years is 50 units. No consensus exists concerning the dose of botulinum toxin that should be used in younger patients. Hypothesis: lower dose of botulinum toxin is sufficient to give good and long lasting results in young patients. The objective of this randomized open-label study is to evaluate the effect of lower doses of Botulinum toxin on the facial rythides in young patients.

详细描述

Botulinum toxin is approved by the FDA for the treatment of facial wrinkles. Patients are usually older than 45 years and their main demand is to treat pre-existing facial wrinkles. However with the increasing popularity of this technique, younger patients, aged 25 to 35 years, are now seeking botulinum toxin injection as a preventive measure for rhytides. The usual dose used for the treatment of facial rhytides in a female patient older than 45 years is 50 units. No consensus exists concerning the dose of botulinum toxin that should be used in younger patients. Hypothesis: lower dose of botulinum toxin is sufficient to give good and long lasting results in young patients.

The objective of this randomized open-label study is to evaluate the effect of lower doses of Botulinum toxin on the facial rythides in young patients.

In this trial, patients will be divided into 3 groups: Group 1 patients will be 25-35 years old and will be injected with 30 units of botulinum toxin into the upper face, group 2 patients will be older than 45 and will be injected with the same amount of botulinum toxin into the upper face and group 3 patients will be older than 45 and will be treated with the usual 50 units dose (control group). Patients older than 45 will be randomized between groups 2 and 3. Validated photonumeric scales will be used to evaluate the wrinkles at rest and with muscle contraction at 2, 4, 8, 12, 16, 20, 24 weeks post injection in the 3 groups. The patient satisfaction rate and the Physician global assessment will also be evaluated in the 3 groups. The scores will be determined by 3 independent blinded raters.

Hypothesis

(1) the low dose will be sufficient to treat the group 1 patients and it will be insufficient to treat the group 2 patients. (2) The results will last longer in groups 1 and 3 patients compared to group 2 patients. (3) Group 1 patients treated with low doses of botulinum toxin will have similar results to the group 3 patients treated with the standard dose of botulinum toxin.

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
Single (Outcomes Assessor)

入排标准

年龄范围
25 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • female patients presenting to our clinic for Facial wrinkle treatment with botulinum toxin
  • Must be between 25-35 years old to be included in group
  • Must be older than 45 to be included in groups 2 and 3.

排除标准

  • Patients with previous periorbital/forehead surgery
  • Patients who plucked the upper eyebrow margin
  • Patients with eyebrow tatoos
  • Patients with upper face botulinum toxin injection in the past 12 months
  • Patients with resorbable upper face fillers injection in the past 12 months
  • Patients with previous permanent upper face fillers injection
  • Pregnant patients
  • Lactating patients
  • Patients with preexisting neuromuscular conditions (myasthenia gravis, Eaton Lambert syndrome)
  • Patients using medication that could potentiate the effect of botulinum (ex: aminoglycoside antibiotics)
  • Patients with sensitivity to botulinum toxin or human albumin

研究组 & 干预措施

Low dose young subjects

Experimental

Group 1 patients will be 25-35 years old and will be injected with 30 units of botulinum toxin into the upper face

干预措施: 30 Units of botulinum toxin (Drug)

Low dose older subjects

Experimental

Group 2 patients will be older than 45 and will be injected with 30 units of botulinum toxin into the upper face

干预措施: 30 Units of botulinum toxin (Drug)

high dose older subjects

Active Comparator

Group 3 patients will be older than 45 and will be treated with the usual 50 units dose into the upper face (control group)

干预措施: 50 Units of botulinum toxin (Drug)

结局指标

主要结局

Changes of scores of Validated photonumeric scales: Brow Positioning Scale at rest

时间窗: 0, 2, 4, 8, 12, 16, 20, 24 weeks

0-Youthful, refreshed look and high-arch eyebrow 1. Medium-arch eyebrow 2. Slight arch of the eyebrow 3. Flat arch of the eyebrow, visibility of folds, and tired appearance 4. Flat eyebrow with barely any arch, marked visibility of folds, and very tired appearance.

Changes of scores of Validated photonumeric scales: Glabellar Lines Scale at rest

时间窗: 0, 2, 4, 8, 12, 16, 20, 24 weeks

0-No glabella lines 1. Mild glabella lines 2. Moderate glabella lines 3. Severe glabella lines 4. Very severe glabella lines

Changes of scores of Validated photonumeric scales: Glabellar Lines Scale with contraction

时间窗: 0, 2, 4, 8, 12, 16, 20, 24 weeks

0-No glabella lines 1. Mild glabella lines 2. Moderate glabella lines 3. Severe glabella lines 4. Very severe glabella lines

Changes of scores of Validated photonumeric scales: Crow Feet Scale with contraction

时间窗: 0, 2, 4, 8, 12, 16, 20, 24 weeks

0-No wrinkles 1. Mild wrinkles 2. Moderate wrinkles 3. Severe wrinkles 4. Very severe wrinkles

Changes of scores of Validated photonumeric scales: Forehead Lines Scale at rest

时间窗: 0, 2, 4, 8, 12, 16, 20, 24 weeks

0-None 1. Minimal 2. Moderate 3. Deep 4. Extreme

Changes of scores of Validated photonumeric scales: Forehead Lines Scale with contraction

时间窗: 0, 2, 4, 8, 12, 16, 20, 24 weeks

0-None 1. Minimal 2. Moderate 3. Deep 4. Extreme

Changes of scores of Validated photonumeric scales: Crow Feet Scale at rest

时间窗: 0, 2, 4, 8, 12, 16, 20, 24 weeks

0-No wrinkles 1. Mild wrinkles 2. Moderate wrinkles 3. Severe wrinkles 4. Very severe wrinkles

次要结局

  • Investigators Global Aesthetic Improvement Scale(0, 2, 4, 8, 12, 16, 20, 24 weeks)
  • Patient satisfaction(0, 2, 4, 8, 12, 16, 20, 24 weeks)

研究者

发起方
St Joseph University, Beirut, Lebanon
申办方类型
Other
责任方
Principal Investigator
主要研究者

samer jabbour

Resident

St Joseph University, Beirut, Lebanon

研究点 (1)

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