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Clinical Trial Summary

To characterize the phenotype in patients with Morton's neuroma and to explore the effect of local administration of Xylocaine (lidocaine)


Clinical Trial Description

A randomised, double-blind, placebo-controlled, three-way cross-over single center study to characterize the phenotype in patients with Morton's Neuroma and to explore the effect of local administration of Xylocaine (lidocaine) ;


Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Basic Science


Related Conditions & MeSH terms


NCT number NCT01298310
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 0
Start date February 2011
Completion date May 2012

See also
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Recruiting NCT05695339 - Resiniferatoxin for the Management of Refractory Morton s Neuroma Pain Phase 1
Recruiting NCT00284583 - Comparison of Alcohol and Steroid Injection for Treating Morton's Neuroma N/A
Completed NCT02550756 - Study to Evaluate the Safety and Tolerability of CNTX-4975 in Subjects With Painful Intermetatarsal Neuroma (Morton's Neuroma) Phase 1
Completed NCT02678793 - A Study to Evaluate the Safety and Efficacy of CNTX-4975 in Subjects With Painful Intermetatarsal Neuroma (Morton's Neuroma) Phase 2
Active, not recruiting NCT05604144 - Cryoanalgesia for the Treatment of Pain in Subjects With Morton's Neuroma N/A