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Clinical Trial Summary

Primary: To compare the analgesic effect over 12 weeks of topical 2PX in stump pain.

Secondary: To prospectively measure other efficacy and safety variables of topical 2PX in stump pain. Exploratory analyses will be performed to measure efficacy and safety variables of topical 2PX in phantom pain


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00804375
Study type Interventional
Source Smerud Medical Research International AS
Contact Robert Macnair, PhD
Phone +44 1357 523481
Email bob.macnair@smerud.com
Status Recruiting
Phase Phase 2
Start date December 2008
Completion date June 2010

See also
  Status Clinical Trial Phase
Active, not recruiting NCT02221934 - Electrical Nerve Block for Amputation Pain N/A
Completed NCT03317600 - Postamputation Pain: Peripheral Mechanisms N/A
Terminated NCT00768248 - Naval Medical Center San Diego (NMCSD) - Ambulatory Continuous Peripheral Nerve Blocks for Treatment of Post-Amputation Phantom Limb and Stump Pain N/A
Terminated NCT00771862 - Prevention of Phantom Limb and Stump Pain Using Ambulatory Continuous Peripheral Nerve Blocks: A Pilot Study Phase 4
Completed NCT00667264 - Ambulatory Continuous Peripheral Nerve Blocks for Treatment of Post-Amputation Phantom Limb and Stump Pain N/A
Completed NCT00462566 - The Efficacy of Motor Cortex Stimulation for Pain Control N/A