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Authors
Bruun, Karin Due https://orcid.org/0000-0002-3106-2461
Christensen, Robin https://orcid.org/0000-0002-6600-0631
Amris, Kirstine https://orcid.org/0000-0003-0792-505X
Blichfeldt-Eckhardt, Morten Rune https://orcid.org/0000-0002-7759-5642
Bye-Møller, Lars
Henriksen, Marius https://orcid.org/0000-0003-1091-2962
Alkjaer, Tine https://orcid.org/0000-0002-9105-3882
Toft, Palle https://orcid.org/0000-0002-3188-449X
Holsgaard-Larsen, Anders https://orcid.org/0000-0003-4106-6930
Vaegter, Henrik Bjarke https://orcid.org/0000-0002-7707-9947
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Clinical Trials BETA
Clinical trials referenced in this document:
nct0427877 at ClinicalTrials.govDocuments that mention this clinical trial
Effect of Naltrexone on Spinal and Supraspinal Pain Mechanisms and Functional Capacity in Women with Fibromyalgia: Exploratory Outcomes from the Randomized Placebo-Controlled FINAL Trial
https://doi.org/10.1007/s40263-025-01183-7
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Funding
Funding for this research was provided by:
Gigtforeningen (A6158)
Aase og Ejnar Danielsens Fond (21-10-0037)
Odense Universitetshospital (A3650)
Odense University Hospital
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Article History
Accepted: 26 March 2025
First Online: 11 April 2025
Declarations
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: Open access funding provided by Odense University Hospital. The Danish Rheumatism Association (A6158), Odense University Hospital’s PhD fund (A3650), and Danielsen’s fund (21-10-0037) supported the study. The Parker Institute, Bispebjerg, and Frederiksberg Hospital are supported by a core grant from the Oak Foundation (OFIL-24-074). The funders had no role in the study’s conception and design, the data interpretation, or the writing of the report.
: No actual or potential conflicts of interest exist for any of the authors (K.D.B., R.C., K.A., M.R.B.-E., L.B.-M., M.H., T.A., P.T., A.H.-L., and H.V.).
: The study received approval from The Ethical Committee of Southern Denmark (S-20190133), the Danish Health and Medicines Authority (19/26406) and was reported to The Danish Data Protection Agency. All procedures in the study adhered to the principles of the Helsinki Declaration.
: Written informed consent was obtained from all participants before their inclusion in the study.
: Not applicable.
: All authors contributed to the study’s conception and design. Study nurse Eva McGehee performed data collection, and Henrik Bjarke Vaegter performed the analysis. Karin Due Bruun wrote the first draft of the manuscript, and all others contributed to revising it. All authors read and approved the final version of the manuscript.
: De-identified data can be acquired, preceded by a signed data access agreement form.
: Not applicable.
