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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04302935
Other study ID # P&E
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 2, 2020
Est. completion date March 2021

Study information

Verified date March 2020
Source Universitair Ziekenhuis Brussel
Contact Maarten Moens, prof. dr.
Phone +32 2 477 55 14
Email maarten.moens@uzbrussel.be
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Full assessment of chronic pain patients based on the ICF-model.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date March 2021
Est. primary completion date March 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with chronic pain for at least 3 months

- Age => 18 years

- Patient has been informed of the study procedures and has given written informed consent

Exclusion Criteria:

- Healthy patients or patients with acute pain.

- Addiction to drugs, alcohol (>5 units per day)

- Evidence of an active disruptive psychiatric disorder that may impact perception of pain, and/or ability to evaluate treatment outcome as determined by investigator

- Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Global pain-assessment
Global pain-assessment, based on the ICF framework

Locations

Country Name City State
Belgium Universitair Ziekenhuis Brussel Jette Brussel

Sponsors (1)

Lead Sponsor Collaborator
Moens Maarten

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility of a global pain-assessment (i.e. practical use) at the time of the assessment: one day (cross-sectional)
Secondary norm values for chronic pain patients on all aspects of the global pain-assessment will be reported (i.e. descriptives) Reporting of norm values on the different aspects of the ICF framework in patients with chronic pain at the time of the assessment: one day (cross-sectional)
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