Browlift Clinical Trial
Official title:
The Impact of Botulinum Toxin Injection in the Frontalis on Brow Height and Morphology: A Randomized Trial
| Verified date | June 2017 |
| Source | St Joseph University, Beirut, Lebanon |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The botulinum toxin was first identified in the late 19th century(1). With its 40 different subtype this toxin is produced mainly by the gram positive anaerobic bacteria Clostridium Botulinum(2). This neurotoxin has great affinity to the neuro muscular junction preventing neurotransmitter release in the synaptic space of acetylcholine(3). The first clinical use was reported by Alan Scott in 1980(4). The most commonly used subtype is toxin A commercially found as BOTOX (onabotulinumtoxinA, Allergan, approved by FDA in 1989), Dysport (abobotulinumtoxinA, Medicis, approved by FDA in 2009) and Xeomin (incobotulinumtoxinA, Merz, approved by FDA in 2010). As for other commercial toxins botulinum neurotoxin serotype B product (MYOBLOC™). Neurotoxin Blast generally 12-15 weeks compared to 3-6 month for neurotoxin A. the FDA approved its use for strabismus in 1989(5), blepharospasm and hemifacial spasm in 1990(6,7), cervical dystonia in 2000(8), glabella in 2000, hyperhidrosis in 2004(9), chronic migrane and detrusor overactiviy in 2014. Other off-label uses have emerged like lanyngeal dysponia, chronic pain etc… (10). Multiple studies with a reduced number of patients have aimed to quantify the effect of botulinum toxin on brow higth. Some studies used injections only to the lateral part of the orbicularis,while others added a corrugator injection. We aimed in this study to compare a known techniques in brow lifting and associanting that with 2 frontalis injection techniques. The main objective is to evaluate the shape of the brow and the elevation in multiple brow landmarks before and after the injection and to see if the frontalis botulinum bloc causes brow ptosis
| Status | Not yet recruiting |
| Enrollment | 30 |
| Est. completion date | August 1, 2017 |
| Est. primary completion date | August 1, 2017 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Female |
| Age group | 30 Years to 60 Years |
| Eligibility |
Inclusion Criteria: 1. Consecutive 30 female patients presenting to our clinic for brow lifting with botulinum toxin will be randomized to receive one of the two injection techniques 2. 30 Years to 60 Years 3. Female Exclusion Criteria: 1. Patients with previous periorbital/forehead surgery 2. Patients who plucked the upper eyebrow margin 3. Patients with eyebrow tatoos 4. Patients with upper face botulinum toxin injection in the past 12 months 5. Patients with resorbable upper face fillers injection in the past 12 months 6. Patients with previous permanent upper face fillers injection 7. Pregnant patients 8. Lactating patients 9. Patients with preexisting neuromuscular conditions (myasthenia gravis, Eaton Lambert syndrome) 10. Patients using medication that could potentiate the effect of botulinum (ex: aminoglycoside antibiotics) 11. Patients with sensitivity to botulinum toxin or human albumin |
| Country | Name | City | State |
|---|---|---|---|
| Lebanon | Saint Joseph University | Beirut |
| Lead Sponsor | Collaborator |
|---|---|
| St Joseph University, Beirut, Lebanon |
Lebanon,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Objective assessment | Objective assessment will be done on anteroposterior views of pre-and-post injection photographs. The mid pupillary line will be drawn and the eyebrow vertical height will be measured from this line to the upper border of the brow at seven horizontal points: the most medial aspect of the eyebrow, medial canthus, and medial limbus, mid pupil, lateral limbus, lateral canthus, and most lateral eyebrow. | 2 weeks | |
| Secondary | 1-Investigators Global Aesthetic Improvement Scale | Improvement in Overall appearance of the upper face, as assessed by the 3 investigators (2 plastic surgeons and 1 dermatologist) using the Global Aesthetic Improvement Scale (GAIS). GAIS will be completed based on photographic assessment comparing post-treatment photos taken at day 15 post intervention to baseline photos (the lower eyelids and lower face will be cropped), to assess overall aesthetic improvement. The GAIS is a 5-point scale (1-5) as follows: Very Much Improved: optimal cosmetic results Much Improved: marked improvement in appearance from initial condition but not completely optimal Improved: obvious improvement in appearance from initial condition but additional treatments are advised No Change: the appearance is the same as the original condition Wose: the appearance is worse from the original condition |
2 weeks | |
| Secondary | 2-Patient satisfaction | Patient satisfaction will be determined by a questionnaire completed at 15 days post-treatment. Subjects will indicate how satisfied they are on a 4-point scale (1-4) as follow: Very Satisfied Satisfied Dissatisfied Very Dissatisfied. |
2 weeks | |
| Secondary | 3-Brow Positioning Scale | subjective evaluation using a photonumeric validated scale for eye brow positioning (evaluated by 2 plastic surgeons and 1 dermatologist) using pre and post injection photographs (taken at day 15 and 30) as follow: 0-Youthful, refreshed look and high-arch eyebrow Medium-arch eyebrow Slight arch of the eyebrow Flat arch of the eyebrow, visibility of folds, and tired appearance Flat eyebrow with barely any arch, marked visibility of folds, and very tired appearance |
2 weeks | |
| Secondary | 4-Forehead Lines Scale: | subjective evaluation using a photonumeric validated scale for forehead lines at rest (evaluated by 2 plastic surgeons and 1 dermatologist) using pre and post injection photographs (taken at day 15 and 30) as follow: 0-None Minimal Moderate Deep Extreme |
2 weeks | |
| Secondary | 5-Glabellar Lines Scale | subjective evaluation using a photonumeric validated scale for glabella lines at rest (evaluated by 2 plastic surgeons and 1 dermatologist) using pre and post injection photographs (taken at day 15) as follow: 0-No glabella lines Mild glabella lines Moderate glabella lines Severe glabella lines Very severe glabella lines |
2 weeks |