Recruitment

Recruitment Status
Completed

Inclusion Criteria

at least 6 months pain duration
written informed consent
diagnosed with any chronic pain condition
at least 6 months pain duration
written informed consent
diagnosed with any chronic pain condition

Exclusion Criteria

participation in any other clinical study
participation in any other clinical study

Summary

Conditions
Chronic Pain
Type
Interventional
Design
  • Allocation: N/A
  • Intervention Model: Single Group Assignment
  • Masking: None (Open Label)
  • Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 75 years
Gender
Both males and females

Inclusion Criteria

at least 6 months pain duration
written informed consent
diagnosed with any chronic pain condition
at least 6 months pain duration
written informed consent
diagnosed with any chronic pain condition

Exclusion Criteria

participation in any other clinical study
participation in any other clinical study

Tracking Information

NCT #
NCT02038244
Collaborators
University of Witten/Herdecke
Investigators
Not Provided