Efficacy and Safety of Prabotulinumtoxin A and Onabotulinumtoxin A for Crow's Feet: A Phase 3, Multicenter, Randomized, Double-Blind, Split-Face Study
Dermatologic Surgery, ISSN: 1524-4725, Vol: 45, Issue: 12, Page: 1610-1619
2019
- 17Citations
- 48Captures
- 95Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations17
- Citation Indexes16
- 16
- CrossRef14
- Policy Citations1
- Policy Citation1
- Captures48
- Readers48
- 48
- Mentions95
- News Mentions95
- News95
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Article Description
BACKGROUND Prabotulinumtoxin A has been shown to have efficacy for the treatment of upper-limb spasticity and improvement of moderate to severe glabellar lines. However, the efficacy and safety of prabotulinumtoxin A for crow's feet have not been evaluated.OBJECTIVEThis study compared the efficacy and safety of prabotulinumtoxin A and onabotulinumtoxin A in the treatment of crow's feet.PATIENTS AND METHODSA multicenter, randomized, double-blind, active-controlled, split-face study was conducted in subjects with bilateral symmetric, moderate to severe crow's feet at maximum smile. The investigators assessed the severity of crow's feet by using the facial wrinkle scale, and the subjects reported the improvement in severity, their subjective satisfaction, and perceived age. The primary efficacy outcome was the proportion of subjects with Grade 0 or 1 severity of crow's feet at maximum smile at Week 4 as assessed by the investigators.RESULTSIn the primary efficacy outcome assessment, there was no significant difference between the 2 groups (prabotulinumtoxin A, 65.02%; onabotulinumtoxin A, 62.56%; p =.0956). All secondary efficacy outcomes were also achieved. Adverse events related to injection were mild and recovered spontaneously.CONCLUSIONPrabotulinumtoxin A and onabotulinumtoxin A have comparable efficacy and safety in the treatment of crow's feet.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85075005979&origin=inward; http://dx.doi.org/10.1097/dss.0000000000001920; http://www.ncbi.nlm.nih.gov/pubmed/30893169; https://journals.lww.com/10.1097/DSS.0000000000001920; https://dx.doi.org/10.1097/dss.0000000000001920; https://journals.lww.com/dermatologicsurgery/Abstract/2019/12000/Efficacy_and_Safety_of_Prabotulinumtoxin_A_and.24.aspx
Ovid Technologies (Wolters Kluwer Health)
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