Patient Satisfaction With Treatment of BOTOX® Cosmetic for the Temporary Correction of Moderate to Severe Glabellar Lines
Completed · Phase 4
Conditions studied: Skin Aging
In brief
This study evaluates the patient satisfaction and onset of effect following treatment with botulinum toxin Type A in the treatment of glabellar rhytids (frown lines)
Key facts
- Study ID
- NCT00856414
- Run by
- Allergan
- People needed
- 45
- Starts
- 2009-03-01
- Expected to finish
- 2009-04-01
- Last updated by the study team
- 2019-01-29
Who can join
Age: 35 and older, up to 55. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Female subjects of any race, 35-55 years of age
- Moderate to severe glabellar wrinkles (lines between the eyebrows)
You may not qualify if…
- Previous botulinum toxin therapy
- Subjects who are pregnant, breast-feeding, or who are of childbearing potential and not practicing a reliable method of birth control
- Subjects planning a facial cosmetic procedure or visible scars
- Previous cosmetic surgery to the upper face
- Medical condition that may increase their risk of exposure to botulinum toxin including diagnosed Myasthenia Gravis, Eaton-Lambert Syndrome, Amyotrophic Lateral Sclerosis, or any other disease that might interfere with neuromuscular function
- History of facial nerve palsy
- Allergy or sensitivity to any component of the study medication
Where it is running
- Study site — West Palm Beach, Florida, United States
- Study site — Livonia, Michigan, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.