Indrekvam, Kari http://orcid.org/0000-0002-9636-9712
Bånerud, Ingrid Fjeldheim
Hermansen, Erland
Austevoll, Ivar Magne
Rekeland, Frode
Guddal, Maren Hjelle
Solberg, Tore K.
Brox, Jens Ivar
Hellum, Christian
Storheim, Kjersti
Clinical trials referenced in this document:
Documents that mention this clinical trial
The Norwegian degenerative spondylolisthesis and spinal stenosis (NORDSTEN) study: study overview, organization structure and study population
https://doi.org/10.1007/s00586-023-07827-w
Comparable increases in dural sac area after three different posterior decompression techniques for lumbar spinal stenosis: radiological results from a randomized controlled trial in the NORDSTEN study
https://doi.org/10.1007/s00586-020-06499-0
Clinical and MRI findings in lumbar spinal stenosis: baseline data from the NORDSTEN study
https://doi.org/10.1007/s00586-021-07051-4
Documents that mention this clinical trial
The Norwegian degenerative spondylolisthesis and spinal stenosis (NORDSTEN) study: study overview, organization structure and study population
https://doi.org/10.1007/s00586-023-07827-w
Decompression alone or with fusion for degenerative lumbar spondylolisthesis (Nordsten-DS): five year follow-up of a randomised, multicentre, non-inferiority trial
https://doi.org/10.1136/bmj-2024-079771
Documents that mention this clinical trial
The Norwegian degenerative spondylolisthesis and spinal stenosis (NORDSTEN) study: study overview, organization structure and study population
https://doi.org/10.1007/s00586-023-07827-w
Funding for this research was provided by:
Helse Vest
Helse Midt-Norge
University of Bergen
Article History
Received: 11 January 2023
Revised: 10 May 2023
Accepted: 12 June 2023
First Online: 3 July 2023
Declarations
:
: The authors have no relevant financial or nonfinancial interest to disclose.
: The Norwegian Committees for Medical and Health Research Ethics approved the trials (NORDTEN-SST trial and NORDSTEN-OC; 2011/2034, NORDSTEN-DS trial; 2013/366). Data protection was approved by the Norwegian Data Inspectorate and data are stored at “Services for sensitive data” (TSD) hosted by the University of Oslo, to allow secure data sharing between researchers. The study was performed according to the Helsinki Declaration and registered at ClinicalTrials.gov under the following identifiers; SST: NCT02007083 10/12/2013 / DS: NCT02051374 31/01/2014/OC: NCT03562936 20/06/2018. The trial is monitored according to requirements of the Good Clinical Practice (GCP) guidelines.
: Informed consent was obtained from patients included in the study after oral and written information.