Recruitment

Recruitment Status
Completed

Inclusion Criterias

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

Exclusion Criterias

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 Criterias

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

Exclusion Criterias

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

Locations

Essen
Essen

Tracking Information

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