Clinical trial

Efficacy and Safety of Intranasal Morphine for Pain After Bunion Surgery

NCT00388011 · Javelin Pharmaceuticals, Industry · Completed

Key facts

NCT number NCT00388011
Title Efficacy and Safety of Intranasal Morphine for Pain After Bunion Surgery
Official title Randomized, Double-Blind, Placebo and Comparator-Controlled, Dose-Response Trial of the Efficacy and Safety of Intranasal Morphine, Intravenous Morphine and Placebo in Patients With Moderate to Severe Pain Following Orthopedic Surgery
Lead sponsor Javelin Pharmaceuticals, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Hallux Valgus
Intervention type Drug
Interventions Intranasal Morphine (MNS075) 3.75 mg, Intravenous Morphine 7.5 mg, Intranasal morphine (MNS075) 7.5 mg, Intranasal morphine (MNS075) 15 mg, Intranasal morphine (MNS075) 30 mg, Intranasal placebo
Enrollment 187
Start date Jan 1, 2005
Primary completion Aug 1, 2005
Completion Aug 1, 2005
First posted Oct 13, 2006
Last update posted Jan 14, 2008

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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