Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
44

Summary

Conditions
  • Brachial Plexus Avulsion
  • Facial Pain
  • Neuropathic Pain
  • Phantom Limb Pain of the Upper Extremities
  • Post Stroke Pain
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Crossover AssignmentMasking: Triple (Participant, Investigator, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 21 years and 70 years
Gender
Both males and females

Description

Prospective, controlled, double blind, randomized, crossover study with endpoint evaluations at the end of each 3-month treatment period. An interim analysis will be conducted by a blinded committee when approximately half of the patients have finished the study.

Prospective, controlled, double blind, randomized, crossover study with endpoint evaluations at the end of each 3-month treatment period. An interim analysis will be conducted by a blinded committee when approximately half of the patients have finished the study.

Tracking Information

NCT #
NCT01554332
Collaborators
Not Provided
Investigators
Study Director: Edward Karst Abbott Neuromodulation