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Eyelash Hypotrichosis clinical trials

View clinical trials related to Eyelash Hypotrichosis.

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NCT ID: NCT02505776 Completed - Clinical trials for Eyelash Hypotrichosis

Safety and Patient Satisfaction With GLASH VISTA™ (Bimatoprost 0.03%) in the Treatment of Eyelash Hypotrichosis in Japan

Start date: December 8, 2014
Phase:
Study type: Observational

This is a post-marketing surveillance study in Japan that will evaluate the safety and patient satisfaction with GLASH VISTA™ (bimatoprost cutaneous solution 0.03%) in the treatment of hypotrichosis of the eyelashes.

NCT ID: NCT01623479 Completed - Clinical trials for Eyelash Hypotrichosis

An Observational Study of Patients Treated With Bimatoprost 0.03% (Latisse®) for Hypotrichosis of the Eyelashes

Start date: November 19, 2010
Phase:
Study type: Observational

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

NCT ID: NCT01391286 Completed - Clinical trials for Eyelash Hypotrichosis

Safety and Efficacy Study of Bimatoprost in Japanese Patients With Chemotherapy-Induced Eyelash Hypotrichosis

Start date: July 1, 2011
Phase: Phase 3
Study type: Interventional

This study will evaluate the safety and efficacy of bimatoprost solution 0.03% compared with vehicle in Japanese adults with hypotrichosis of the eyelashes following chemotherapy treatment.

NCT ID: NCT01391273 Completed - Clinical trials for Eyelash Hypotrichosis

Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypotrichosis

Start date: July 1, 2011
Phase: Phase 3
Study type: Interventional

This study will evaluate the safety and efficacy of bimatoprost solution 0.03% compared with vehicle in Japanese adults with hypotrichosis of the eyelashes.

NCT ID: NCT01229423 Completed - Clinical trials for Eyelash Hypotrichosis

Safety and Efficacy of LATISSE® in the Augmentation of Eyelashes of Korean Subjects

Start date: November 2009
Phase: Phase 4
Study type: Interventional

This study will evaluate the safety and efficacy of LATISSE® (bimatoprost 0.03%) in the augmentation of eyelashes in Korean women.

NCT ID: NCT01064882 Completed - Clinical trials for Eyelash Hypotrichosis

Safety and Efficacy of Bimatoprost Ophthalmic Solution in Increasing Eyelash Prominence

Start date: March 2010
Phase: Phase 2
Study type: Interventional

This study will evaluate the safety and efficacy of bimatoprost ophthalmic solution 0.005% or 0.015% compared with bimatoprost ophthalmic solution 0.03% once-daily application to the upper eyelid margins in increasing eyelash prominence

NCT ID: NCT01023841 Completed - Alopecia Areata Clinical Trials

Safety and Efficacy of Bimatoprost Solution in Treating Eyelash Loss or Hypotrichosis in Children

Start date: June 1, 2010
Phase: Phase 4
Study type: Interventional

This study will evaluate the safety and efficacy of bimatoprost solution 0.03% once daily application to the upper eyelid margins compared with vehicle in treating eyelash loss or hypotrichosis (inadequate or not enough eyelashes) in children.