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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04657159
Other study ID # IPM-PRP2020
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2020
Est. completion date September 30, 2022

Study information

Verified date July 2022
Source Eques Indolor AB
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The overall aim of the study is to evaluate interventional pain management. This is done in three steps: 1. To find matched controls to the patients in the study on cost-effectiveness of IPM and compare the results. 2. To calculate cost-effectiveness of PRP during the period 2010-2016, on a national level. 3. To calculate cost-effectiveness of PRP during the period 2017-2019, after the changed guidelines for PRP in Sweden. The two last steps are to provide a background to the results of IPM, and to see if the results in the subgroup of matched controls of PRP-patients differ from the results from the whole population.


Description:

Chronic pain is one of the major health problems globally, according to the WHO 'global burden of disease' studies. Previously, the investigators have performed a study on a feasible approach to be able to treat zygapophyseal joint pain in the thoracic region, similar to the established methods for treatment in the lumbar and cervical regions which have been published. The study showed that there was a significant improvement in health related quality of life (HRQoL) after treatment, and that there were no difference in the results depending on if it was the cervical, thoracic or lumbar region that was treated. The study had ethical approval (Dnr 2012-446-31M) and is registered here at clinicaltrials.gov. Another study explored the health economic aspects of interventional pain management (IPM). The investigators aimed to do this in comparison with pain rehabilitation programs, and therefore further ethical approval was searched and gained (2012-446-31M, 2017-542-32, 2018- 507-32) An health-economic evaluation of only IPM was performed showing that patients after treatment of diagnosed pain-focuses in zygapophyseal joint pain not only improve their HRQoL but they also reduce their medication, reduced their health-care consumption and gained in ability to work. The cost per quality adjusted life years gained was below the threshold for cost-effective health-care according to the threshold-levels defined by the national Board of Health and Welfare in Sweden. But the investigators need a larger population to select from in order to get matched controls among patients that have been through pain rehabilitation programs. This study therefore aims to explore the national register of pain rehabilitation both in order to find matched controls and in order to make a cost-effectiveness study of pain rehabilitation program as it is performed in Sweden.


Recruitment information / eligibility

Status Completed
Enrollment 15611
Est. completion date September 30, 2022
Est. primary completion date December 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 94 Years
Eligibility Inclusion Criteria: Been through pain rehabilitation program Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pain rehabilitation program
Effect on health related quality of life och health-care consumption after rehabilitation

Locations

Country Name City State
Sweden Department of Epidemiology and Global Health Umeå University Umeå
Sweden Smärtkliniken Eques Indolor Vallentuna

Sponsors (2)

Lead Sponsor Collaborator
Eques Indolor AB Umeå University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Health-related quality of life EQ-5D index 1 year
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