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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02936245
Other study ID # PONH CSM
Secondary ID
Status Recruiting
Phase N/A
First received October 12, 2016
Last updated October 14, 2016
Start date October 2013
Est. completion date July 2020

Study information

Verified date October 2016
Source Shanghai University of Traditional Chinese Medicine
Contact Cui / Xue-jun, PhD
Phone 18917763017
Email 13917715524@139.com
Is FDA regulated No
Health authority China: Shanghai Municipal Commission of Health and Family Planning
Study type Observational

Clinical Trial Summary

Cervical spondylotic myelopathy (CSM) is the most frequent cause of myelopathy in those over the age of 50. They claim that surgical treatment of myelopathy, especially of the mild and moderate forms, has not shown better results than conservative treatment in the long term, and criteria for the indication and the timing of the operation have not been established. In order to get some more reliable data, a long-term follow up observational study will be started to confirm the effects of long term for conservative treatment.


Description:

Cervical spondylotic myelopathy (CSM) is the most frequent cause of myelopathy in those over the age of 50 [1]. It is believed to have a generally progressive course over a period of years, with sudden acceleration especially following a slight head and neck injury, leading to significant disability [2, 3]. The treatment of CSM remains a problem, particularly in the mild and moderate forms without rapid progression.

Excellent outcomes for surgery have been presented in many studies. All of the studies, however, are retrospective, and many lack a clear design, standard criteria, control groups, and sufficient follow-up, so it is difficult to compare [4, 5, 6]. Furthermore, several studies and critical reviews are not so optimistic. They claim that surgical treatment of myelopathy, especially of the mild and moderate forms, has not shown better results than conservative treatment in the long term, and criteria for the indication and the timing of the operation have not been established [7, 8, 9]. Twenty-five percent of patients with laminoplasty suffer from severe neck and shoulder pain for more than 3 months [10], with significant morbidity from the iliac crest donor site etc. Surgery to decompress and stabilize the spine is often advocated for severe or progressive symptoms, with mixed results. About two-thirds of patients improve with surgery, whereas surgery is not successful in 15% to 30% of cases [11].

In order to get some more reliable data, a long-term follow up observational study will be started to confirm the effects of long term for conservative treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 350
Est. completion date July 2020
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

1. Clinical signs and symptoms of cervical cord dysfunction

2. Magnetic resonance imaging (MRI) criteria for cervical multisegmental cord compression and/or myelopathy due to spondylosis (including soft disc herniations) with or without developmentally narrow spinal canal

3. Age under 75 years

4. Patient's consent to conservative treatment It has been suggested that magnetic resonance imaging

Exclusion Criteria:

1. Spinal cord compression, without clinical symptoms

2. Previous surgery on the cervical spine

3. Uncertainty about the presence of significant additional diseases (such as Motor neurone disease, progressive polyarthritis)

4. Cervical cord dysfunction due to tumors, trauma, soft disc herniation or previous surgery

5. Serious that require a surgical procedure

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
no specific intervention
We will not assign specific intervention in this research. We will record their baseline characteristics, received treatment, and assess the outcomes to analysis the predictors of outcome and natural history in patients with cervical spondylotic myelopathy.

Locations

Country Name City State
China Longhua Hospital, Shanghai University of Traditional Chinese Medicine Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai University of Traditional Chinese Medicine

Country where clinical trial is conducted

China, 

References & Publications (3)

Law MD Jr, Bernhardt M, White AA 3rd. Cervical spondylotic myelopathy: a review of surgical indications and decision making. Yale J Biol Med. 1993 May-Jun;66(3):165-77. Review. — View Citation

Rowland LP. Surgical treatment of cervical spondylotic myelopathy: time for a controlled trial. Neurology. 1992 Jan;42(1):5-13. Review. — View Citation

Young WF. Cervical spondylotic myelopathy: a common cause of spinal cord dysfunction in older persons. Am Fam Physician. 2000 Sep 1;62(5):1064-70, 1073. Review. Erratum in: Am Fam Physician 2001 May 15;63(10):1916. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Japanese Orthopaedic Association scale Japanese Orthopaedic Association scale assessed for 3 years 3 years No
Secondary Adverse Event Adverse Event recorded 6 months, 1, 2, 3,4 and 5 years 6 months, 1, 2, 3,4 and 5 years Yes
Secondary Visual Analogue Scale Visual Analogue Scale assessed for 6 months, 1, 2, 3,4 and 5 years 6 months, 1, 2, 3,4 and 5 years No
Secondary the Medical Outcomes Study short form health survey-36 assessed for 6 months, 1, 2, 3,4 and 5 years 6 months, 1, 2, 3,4 and 5 years No
Secondary Neck Disability Index Neck Disability Index assessed for 6 months, 1, 2, 3,4 and 5 years 6 months, 1, 2, 3,4 and 5 years No
Secondary Japanese Orthopaedic Association scale Japanese Orthopaedic Association scale assessed for 6 months, 1, 2, 3,4 and 5 years 6 months, 1, 2, 4 and 5 years No
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