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Clinical Trial Summary

This multi-site Phase 3 clinical trial is a randomized, double-blind, placebo-controlled study to identify the safety and efficacy of DPI 386 nasal gel (intranasal scopolamine gel) for the prevention and treatment of nausea associated with motion sickness. The study will be conducted aboard military ships undergoing military operations or aboard commercial boats rented for the study to obtain data in a real world environment. The study will have three arms: DPI-386 nasal gel, placebo nasal gel, and Transderm Scop® (1.0 mg/72 hours; transdermal scopolamine patch [TDS], the current standard of care for the treatment of motion sickness). The study will include 120 subjects per arm, for a total of 360 subjects (n=360). A double-dummy design will be used to mask the treatment assignment. All subjects will receive both a patch and nasal gel: DPI-386 Nasal Gel + placebo patch, placebo nasal gel + placebo patch, or TDS patch + placebo nasal gel.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Motion Sickness
  • Nausea
  • Prevention of Nausea Associated With Motion Sickness
  • Treatment of Nausea Associated With Motion Sickness

NCT number NCT03920644
Study type Interventional
Source Naval Aeromedical Research Unit, Dayton
Contact Joshua Baker, MS
Phone 9376562473
Email Joshua.baker.16.ctr@us.af.mil
Status Recruiting
Phase Phase 3
Start date April 2019
Completion date March 2021