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Safety and efficacy of riluzole in patients undergoing decompressive surgery for degenerative cervical myelopathy (CSM-Protect): a multicentre, double-blind, placebo-controlled, randomised, phase 3 trial
by
Badhiwala, Jetan H
, Harrop, James S
, Santaguida, Carlo
, Farhadi, H Francis
, Nassr, Ahmad
, Vaccaro, Alexander R
, Fehlings, Michael G
, Yoon, S Tim
, Massicotte, Eric M
, Kopjar, Branko
, Shaffrey, Christopher I
, Mummaneni, Praveen
, Brodke, Darrel S
, Hilibrand, Alan S
, Wilson, Jason
, Arnold, Paul M
, Ahn, Henry
, Jacobs, W Bradley
, Kelly, Michael
, Fourney, Daryl R
, Riew, K Daniel
, Kim, Kee D
in
Adolescent
/ Adult
/ Adverse events
/ Aged
/ Aged, 80 and over
/ Central nervous system diseases
/ Cervical Vertebrae - surgery
/ Combined Modality Therapy
/ Decompression
/ Decompressive Craniectomy - methods
/ Double-Blind Method
/ Double-blind studies
/ Dysphagia
/ Endpoint Determination
/ Female
/ Humans
/ Intervertebral Disc Degeneration - drug therapy
/ Intervertebral Disc Degeneration - surgery
/ Male
/ Middle Aged
/ Neck pain
/ Neuroprotective Agents - adverse effects
/ Neuroprotective Agents - therapeutic use
/ Neurosurgical Procedures - methods
/ Osteoarthritis
/ Pain, Postoperative - epidemiology
/ Patients
/ Pharmacy
/ Placebos
/ Population studies
/ Recovery of function
/ Riluzole - adverse effects
/ Riluzole - therapeutic use
/ Spinal Cord Compression - drug therapy
/ Spinal Cord Compression - surgery
/ Spinal cord injuries
/ Statistical analysis
/ Surgery
/ Treatment Outcome
2021
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Safety and efficacy of riluzole in patients undergoing decompressive surgery for degenerative cervical myelopathy (CSM-Protect): a multicentre, double-blind, placebo-controlled, randomised, phase 3 trial
by
Badhiwala, Jetan H
, Harrop, James S
, Santaguida, Carlo
, Farhadi, H Francis
, Nassr, Ahmad
, Vaccaro, Alexander R
, Fehlings, Michael G
, Yoon, S Tim
, Massicotte, Eric M
, Kopjar, Branko
, Shaffrey, Christopher I
, Mummaneni, Praveen
, Brodke, Darrel S
, Hilibrand, Alan S
, Wilson, Jason
, Arnold, Paul M
, Ahn, Henry
, Jacobs, W Bradley
, Kelly, Michael
, Fourney, Daryl R
, Riew, K Daniel
, Kim, Kee D
in
Adolescent
/ Adult
/ Adverse events
/ Aged
/ Aged, 80 and over
/ Central nervous system diseases
/ Cervical Vertebrae - surgery
/ Combined Modality Therapy
/ Decompression
/ Decompressive Craniectomy - methods
/ Double-Blind Method
/ Double-blind studies
/ Dysphagia
/ Endpoint Determination
/ Female
/ Humans
/ Intervertebral Disc Degeneration - drug therapy
/ Intervertebral Disc Degeneration - surgery
/ Male
/ Middle Aged
/ Neck pain
/ Neuroprotective Agents - adverse effects
/ Neuroprotective Agents - therapeutic use
/ Neurosurgical Procedures - methods
/ Osteoarthritis
/ Pain, Postoperative - epidemiology
/ Patients
/ Pharmacy
/ Placebos
/ Population studies
/ Recovery of function
/ Riluzole - adverse effects
/ Riluzole - therapeutic use
/ Spinal Cord Compression - drug therapy
/ Spinal Cord Compression - surgery
/ Spinal cord injuries
/ Statistical analysis
/ Surgery
/ Treatment Outcome
2021
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Safety and efficacy of riluzole in patients undergoing decompressive surgery for degenerative cervical myelopathy (CSM-Protect): a multicentre, double-blind, placebo-controlled, randomised, phase 3 trial
by
Badhiwala, Jetan H
, Harrop, James S
, Santaguida, Carlo
, Farhadi, H Francis
, Nassr, Ahmad
, Vaccaro, Alexander R
, Fehlings, Michael G
, Yoon, S Tim
, Massicotte, Eric M
, Kopjar, Branko
, Shaffrey, Christopher I
, Mummaneni, Praveen
, Brodke, Darrel S
, Hilibrand, Alan S
, Wilson, Jason
, Arnold, Paul M
, Ahn, Henry
, Jacobs, W Bradley
, Kelly, Michael
, Fourney, Daryl R
, Riew, K Daniel
, Kim, Kee D
in
Adolescent
/ Adult
/ Adverse events
/ Aged
/ Aged, 80 and over
/ Central nervous system diseases
/ Cervical Vertebrae - surgery
/ Combined Modality Therapy
/ Decompression
/ Decompressive Craniectomy - methods
/ Double-Blind Method
/ Double-blind studies
/ Dysphagia
/ Endpoint Determination
/ Female
/ Humans
/ Intervertebral Disc Degeneration - drug therapy
/ Intervertebral Disc Degeneration - surgery
/ Male
/ Middle Aged
/ Neck pain
/ Neuroprotective Agents - adverse effects
/ Neuroprotective Agents - therapeutic use
/ Neurosurgical Procedures - methods
/ Osteoarthritis
/ Pain, Postoperative - epidemiology
/ Patients
/ Pharmacy
/ Placebos
/ Population studies
/ Recovery of function
/ Riluzole - adverse effects
/ Riluzole - therapeutic use
/ Spinal Cord Compression - drug therapy
/ Spinal Cord Compression - surgery
/ Spinal cord injuries
/ Statistical analysis
/ Surgery
/ Treatment Outcome
2021
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Safety and efficacy of riluzole in patients undergoing decompressive surgery for degenerative cervical myelopathy (CSM-Protect): a multicentre, double-blind, placebo-controlled, randomised, phase 3 trial
Journal Article
Safety and efficacy of riluzole in patients undergoing decompressive surgery for degenerative cervical myelopathy (CSM-Protect): a multicentre, double-blind, placebo-controlled, randomised, phase 3 trial
2021
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Overview
Degenerative cervical myelopathy represents the most common form of non-traumatic spinal cord injury. This trial investigated whether riluzole enhances outcomes in patients undergoing decompression surgery for degenerative cervical myelopathy.
This multicentre, double-blind, placebo-controlled, randomised, phase 3 trial was done at 16 university-affiliated centres in Canada and the USA. Patients with moderate-to-severe degenerative cervical myelopathy aged 18–80 years, who had a modified Japanese Orthopaedic Association (mJOA) score of 8–14, were eligible. Patients were randomly assigned (1:1) to receive either oral riluzole (50 mg twice a day for 14 days before surgery and then for 28 days after surgery) or placebo. Randomisation was done using permuted blocks stratified by study site. Patients, physicians, and outcome assessors remained masked to treatment group allocation. The primary endpoint was change in mJOA score from baseline to 6 months in the intention-to-treat (ITT) population, defined as all individuals who underwent randomisation and surgical decompression. Adverse events were analysed in the modified intention-to-treat (mITT) population, defined as all patients who underwent randomisation, including those who did not ultimately undergo surgical decompression. This study is registered with ClinicalTrials.gov, NCT01257828.
From Jan 31, 2012, to May 16, 2017, 408 patients were screened. Of those screened, 300 were eligible (mITT population); 290 patients underwent decompression surgery (ITT population) and received either riluzole (n=141) or placebo (n=149). There was no difference between the riluzole and placebo groups in the primary endpoint of change in mJOA score at 6-month follow-up: 2·45 points (95% CI 2·08 to 2·82 points) versus 2·83 points (2·47 to 3·19), difference −0·38 points (−0·90 to 0·13; p=0·14). The most common adverse events were neck or arm or shoulder pain, arm paraesthesia, dysphagia, and worsening of myelopathy. There were 43 serious adverse events in 33 (22%) of 147 patients in the riluzole group and 34 serious adverse events in 29 (19%) of 153 patients in the placebo group. The most frequent severe adverse events were osteoarthrosis of non-spinal joints, worsening of myelopathy, and wound complications.
In this trial, adjuvant treatment for 6 weeks perioperatively with riluzole did not improve functional recovery beyond decompressive surgery in patients with moderate-to-severe degenerative cervical myelopathy. Whether riluzole has other benefits in this patient population merits further study.
AOSpine North America.
Publisher
Elsevier Ltd,Elsevier Limited
Subject
/ Adult
/ Aged
/ Central nervous system diseases
/ Cervical Vertebrae - surgery
/ Decompressive Craniectomy - methods
/ Female
/ Humans
/ Intervertebral Disc Degeneration - drug therapy
/ Intervertebral Disc Degeneration - surgery
/ Male
/ Neuroprotective Agents - adverse effects
/ Neuroprotective Agents - therapeutic use
/ Neurosurgical Procedures - methods
/ Pain, Postoperative - epidemiology
/ Patients
/ Pharmacy
/ Placebos
/ Spinal Cord Compression - drug therapy
/ Spinal Cord Compression - surgery
/ Surgery
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