Last updated on November 2019

Evaluation of DEX-IN During Outpatient Procedures


Brief description of study

The primary objective of this study is to evaluate the analgesic efficacy of DEX-IN compared with placebo and active control (fentanyl), in subjects undergoing painful outpatient and office based procedures.

Clinical Study Identifier: NCT03348423

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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