Örebro Multicenter Study on Operative Treatment of Cervical Radiculopathy (OMSAP)
Primary Purpose
Cervical Radiculopathy, Cervical Root Compression
Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
ACDF
PF
Sponsored by
About this trial
This is an interventional treatment trial for Cervical Radiculopathy focused on measuring Pain, Nerve root dysfunction, Anterior Cervical Decompression and Fusion, Posterior Foraminotomy
Eligibility Criteria
Inclusion Criteria:
- Symptoms of radiating arm pain with duration of at least six weeks
- Neck disability index (NDI) over 30 points (60%);
- Correlating findings on MRI on one or two cervical levels
- Eligible for both treatments
- Ability to understand and read Swedish.
Exclusion Criteria:
- Previous cervical spine surgery
- More then two cervical levels requiring treatment
- Severe facet joint osteoarthritis
- Symptoms or marked radiologic signs of myelopathy
- Drug abuse
- Dementia or expected low compliance
- Cervical malformation
- Marked instability, 3.5-mm translation or >11 degrees more motion compared to adjacent segments
- History of severe cervical trauma
- Generalized pain syndrome or WAD
- Pregnancy
- Rheumatoid arthritis
- Ankylosing spondylitis
- Malignancy
- Active infection or another severe systemic disease
- Patients that are unsuitable for either intervention deemed by the consultant spine surgeon
Sites / Locations
- Ryggkirurgiskt Centrum StockholmRecruiting
- Norrlands Universitetssjukhus
- Akademiska Sjukhuset UppsalaRecruiting
- Universistessjukhuset ÖrebroRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Anterior Cervical Decompression and Fusion (ACDF)
Posterior Foraminotomy (PF)
Arm Description
Patients entered into this arm are treated via an anterior approach with disk excision, root canal decompression and fusion of the affected segment with a cage and plate.
Patients entered into this arm are treated via a posterior approach through intermuscular planes. The root canal is decompressed by burring the medial third of the facet joint. No fusion is performed.
Outcomes
Primary Outcome Measures
Neck Disablity index, NDI.
Primary variable is NDI change at two year compared to baseline. NDI is a self-administered questionnaire with 10 items measuring disability in patients with neck pain. The questions cover daily activities, such as the ability to dress, lift heavy objects, read, work, drive a car, sleep and perform leisure time activities, as well as the amount of pain, headache and concentration abilities. Each item is scored from 0 to 5. MCID for NDI is 7,5-8,5 or 17,3%.
NDI change will also be measured at different time intervals to highlight the change over time.
Secondary Outcome Measures
EQ-5D
Secondary variable is EQ-5D change at two year compared to baseline. EQ-5D, The European Quality of Life-5 Dimensions (EQ-5D; with a range from approximately -0.5 to 1, with higher scores indicating better quality of life) using the Swedish translation [36, 37].
EQ-5D change will also be measured at different time intervals to highlight the change over time.
NRS neck, NRS arm
Numerical Rating Scale (NRS) for pain is a unidimensional measure of pain intensity in adults. The NRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number 0 no pain to 10 worst pain imaginable that best reflects the intensity of their pain. MCID is 2.2 point for NRS
NRS change will also be measured at different time intervals to highlight the change over time
Full Information
NCT ID
NCT04177849
First Posted
November 19, 2019
Last Updated
May 22, 2022
Sponsor
Region Örebro County
Collaborators
Uppsala University Hospital, Rygglkirurgiskt Centrum Stockholm AB, Norrlands University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04177849
Brief Title
Örebro Multicenter Study on Operative Treatment of Cervical Radiculopathy
Acronym
OMSAP
Official Title
Örebro Multicenter Study on Operative Treatment of Cervical Radiculopathy: Anterior Cervical Decompression and Fusion Versus Posterior Foraminotomy
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 20, 2020 (Actual)
Primary Completion Date
January 2026 (Anticipated)
Study Completion Date
January 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Region Örebro County
Collaborators
Uppsala University Hospital, Rygglkirurgiskt Centrum Stockholm AB, Norrlands University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study compares anterior cervical decompression and fusion (ACDF) to posterior foraminotomy (PF) in surgical treatment for cervical radiculopathy (CR) caused by root canal compression, in a multicenter prospective randomized trial. The investigators hypothesize equal decompression of nerve root, and equal clinical outcome in both treatment groups.
Detailed Description
Both ACDF and PF are effective in surgical treatment of CR. However, the techniques has different complication profiles and carry different costs. No comparative study with high level of evidence has been published, why the basis for clinical guidelines are lacking.
The study consists of 110 patients with CR not responding to non-surgical treatment for 6 weeks and with a Neck Disability Index (NDI) over 30 points/60 %, that are randomized to either technique in a 1:1 ratio and followed for two years.
Primary variable is NDI, secondary variables are Numerical Pain Rating Scale (NRS) separately for arm and neck pain and health related quality of life (EQ-5D). Tertiary variables are complications and reoperations. The patients are also followed radiolgraphically with plain x-rays in extension and flexion, CT, and MRI.
The study has a non-inferiority design with ACDF as active control. A NDI difference of less than 8,5 points/17 % (=minimally clinical important difference, MCID, for NDI) is considered a non-inferior result. A secondary superiority evaluation will also be performed.
Analysis Primarily, patient-related outcome measures will be analyzed in terms of intention to treat (ITT) and include all randomized patients. Missing values will be imputed. The investigators will calculate, by using analysis of covariance (ANCOVA), the mean outcome values for each treatment group, adjusted for baseline values of the outcome. The mean difference between the groups will also be presented.
Secondary outcome analyses using the Student t test, Chi-Square, Mann-Whitney, Fisher exact test.
The tertiary outcome analyses will be based on available cases. The time to revision surgery according to treatment assignment will be analyzed and plotted according to the Kaplan-Meier method, while hazard ratios, with regard to having secondary surgery after ACDF compared to PF, will be estimated by the Cox model with calendar time as the time scale. Men and women will be analyzed separately.
An "Ad Interim" analysis will be performed by a non-partial observer and/or statistician when 40 patients are included, regarding NDI difference, complications and reoperations.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Radiculopathy, Cervical Root Compression
Keywords
Pain, Nerve root dysfunction, Anterior Cervical Decompression and Fusion, Posterior Foraminotomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
110 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Anterior Cervical Decompression and Fusion (ACDF)
Arm Type
Active Comparator
Arm Description
Patients entered into this arm are treated via an anterior approach with disk excision, root canal decompression and fusion of the affected segment with a cage and plate.
Arm Title
Posterior Foraminotomy (PF)
Arm Type
Experimental
Arm Description
Patients entered into this arm are treated via a posterior approach through intermuscular planes. The root canal is decompressed by burring the medial third of the facet joint. No fusion is performed.
Intervention Type
Procedure
Intervention Name(s)
ACDF
Intervention Description
A 4-cm anterolateral transverse incision is made over the index level, on either the right or left side. Platysma is sectioned transversal to its fibers and the anterior aspect of the spinal column is bluntly exposed between the carotid sheath and the esophagus. The disk is excised, including the posterior longitudinal ligament. Disk fragments and/or osteophytes from the uncovertebral joint on the affected side are removed until the root is fully decompressed. Reconstruction is typically done with an interbody spacer, autologous bone graft and a stabilizing plate screwed to the adjacent vertebral bodies. A fusion cage with integrated screws may also be used according to the surgeon's preference.
Intervention Type
Procedure
Intervention Name(s)
PF
Intervention Description
A 4-cm longitudinal midline incision exposes the spinous processes of the adjacent vertebrae. The facet joint covering the index foramen is exposed through intermuscular planes. The root canal is opened as the medial third of the facet joint is removed with a high-speed diamond burr. The affected nerve root is decompressed by laterally undercutting the facet joint throughout its length.
Primary Outcome Measure Information:
Title
Neck Disablity index, NDI.
Description
Primary variable is NDI change at two year compared to baseline. NDI is a self-administered questionnaire with 10 items measuring disability in patients with neck pain. The questions cover daily activities, such as the ability to dress, lift heavy objects, read, work, drive a car, sleep and perform leisure time activities, as well as the amount of pain, headache and concentration abilities. Each item is scored from 0 to 5. MCID for NDI is 7,5-8,5 or 17,3%.
NDI change will also be measured at different time intervals to highlight the change over time.
Time Frame
4-6 weeks, 3 months, 1 year, 2 year, 5 year
Secondary Outcome Measure Information:
Title
EQ-5D
Description
Secondary variable is EQ-5D change at two year compared to baseline. EQ-5D, The European Quality of Life-5 Dimensions (EQ-5D; with a range from approximately -0.5 to 1, with higher scores indicating better quality of life) using the Swedish translation [36, 37].
EQ-5D change will also be measured at different time intervals to highlight the change over time.
Time Frame
4-6 weeks, 3 months, 1 year, 2 year, 5 year
Title
NRS neck, NRS arm
Description
Numerical Rating Scale (NRS) for pain is a unidimensional measure of pain intensity in adults. The NRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number 0 no pain to 10 worst pain imaginable that best reflects the intensity of their pain. MCID is 2.2 point for NRS
NRS change will also be measured at different time intervals to highlight the change over time
Time Frame
4-6 weeks, 3 months, 1 year, 2 year, 5 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Symptoms of radiating arm pain with duration of at least six weeks
Neck disability index (NDI) over 30 points (60%);
Correlating findings on MRI on one or two cervical levels
Eligible for both treatments
Ability to understand and read Swedish.
Exclusion Criteria:
Previous cervical spine surgery
More then two cervical levels requiring treatment
Severe facet joint osteoarthritis
Symptoms or marked radiologic signs of myelopathy
Drug abuse
Dementia or expected low compliance
Cervical malformation
Marked instability, 3.5-mm translation or >11 degrees more motion compared to adjacent segments
History of severe cervical trauma
Generalized pain syndrome or WAD
Pregnancy
Rheumatoid arthritis
Ankylosing spondylitis
Malignancy
Active infection or another severe systemic disease
Patients that are unsuitable for either intervention deemed by the consultant spine surgeon
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marek Holy, MD
Phone
+46 0196025323
Email
marek.holy@regionorebrolan.se
First Name & Middle Initial & Last Name or Official Title & Degree
Claes Olerud, Prof. MD. PhD
Phone
+46 018 611 72 24
Email
claes.olerud@surgsciuu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Per Wretenberg, Prof. MD. PhD
Organizational Affiliation
Region Örebro County
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Claes Olerud, Prof. MD. PhD
Organizational Affiliation
Uppsala University
Official's Role
Study Director
Facility Information:
Facility Name
Ryggkirurgiskt Centrum Stockholm
City
Stockholm
ZIP/Postal Code
114 33
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Martin Skeppsholm, MD. PhD
Phone
+46 08 12458100
Email
martin.skeppholm@RKC.se
Facility Name
Norrlands Universitetssjukhus
City
Umeå
ZIP/Postal Code
90737
Country
Sweden
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lukas Bobinski, MD. PhD
Phone
+46 090 785 00 00
Email
lukas.bobinski@vll.se
Facility Name
Akademiska Sjukhuset Uppsala
City
Uppsala
ZIP/Postal Code
75185
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Claes Olerud, Prof. MD. PhD
Phone
+46 018 611 72 24
Email
claes.olerud@surgsciuu.se
Facility Name
Universistessjukhuset Örebro
City
Örebro
ZIP/Postal Code
701 85
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marek Holy, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34496941
Citation
Holy M, MacDowall A, Sigmundsson FG, Olerud C. Operative treatment of cervical radiculopathy: anterior cervical decompression and fusion compared with posterior foraminotomy: study protocol for a randomized controlled trial. Trials. 2021 Sep 8;22(1):607. doi: 10.1186/s13063-021-05492-2. Erratum In: Trials. 2021 Sep 29;22(1):667.
Results Reference
derived
Learn more about this trial
Örebro Multicenter Study on Operative Treatment of Cervical Radiculopathy
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