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Clinical Trial Summary

The objective of this study is to compare the relative efficacy and safety of the test formulation of ciprofloxacin 0.3%/dexamethasone 0.1% sterile otic suspension (Par Pharmaceutical Companies, Inc.) to the already-marketed formulation CIPRODEX® (ciprofloxacin 0.3%/dexamethasone 0.1%) sterile otic suspension (Alcon) in the treatment of acute bacterial otitis externa.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01910155
Study type Interventional
Source Par Pharmaceutical, Inc.
Contact
Status Terminated
Phase Phase 3
Start date July 2013
Completion date March 2015

See also
  Status Clinical Trial Phase
Terminated NCT00523120 - Topical Voltaren in Otitis Externa Phase 2
Completed NCT00872209 - Safety and Efficacy Study of Foam Otic Cipro Compared to a Standard Solution ( Ciloxan - Alcon Labs ) to Treat Acute Otitis Externa Phase 1/Phase 2
Recruiting NCT05370209 - Performance and Safety of Otinova® Ear Spray N/A
Completed NCT02558738 - Non Interventional Clinical Investigation of Ectoin Ear Spray in Skin Treatment of Outer Ear Canal Irritations N/A
Completed NCT02511561 - OTO-201 for the Treatment of Otitis Externa Phase 2
Completed NCT01359098 - Efficacy and Safety of Once-Daily Ciprodexa Otic Foam Compared to Twice-daily Ciprodex Ear Drops in Acute Otitis Externa Phase 2
Completed NCT01157819 - Safety and Efficacy of Once-Daily Dosing of FoamOtic Cipro Compared to Twice-Daily Dosing of Ciloxan Ear Drops in Patients With Acute External Otitis Phase 2
Completed NCT00980876 - A Comparative Study Between Two Formulations of the Ciprofloxacin Hydrochloride + Hydrocortisone Otic Suspension Phase 3