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Clinical Trial Summary

This is an observational study of patients treated with bimatoprost 0.03% (Latisse®) for at least 12 months for hypotrichosis of the eyelashes.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01623479
Study type Observational
Source Allergan
Contact
Status Completed
Phase
Start date November 19, 2010
Completion date September 1, 2011

See also
  Status Clinical Trial Phase
Completed NCT01229423 - Safety and Efficacy of LATISSE® in the Augmentation of Eyelashes of Korean Subjects Phase 4
Completed NCT01064882 - Safety and Efficacy of Bimatoprost Ophthalmic Solution in Increasing Eyelash Prominence Phase 2
Completed NCT01023841 - Safety and Efficacy of Bimatoprost Solution in Treating Eyelash Loss or Hypotrichosis in Children Phase 4
Completed NCT01391286 - Safety and Efficacy Study of Bimatoprost in Japanese Patients With Chemotherapy-Induced Eyelash Hypotrichosis Phase 3
Completed NCT01391273 - Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypotrichosis Phase 3
Completed NCT02505776 - Safety and Patient Satisfaction With GLASH VISTAâ„¢ (Bimatoprost 0.03%) in the Treatment of Eyelash Hypotrichosis in Japan