Efficacy and Safety of Nerve Root Axial Decompression Surgery in The Treatment of Tethered Cord Syndrome
Primary Purpose
Tethered Cord Syndrome
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Conservative treatment
Capsule surgery
Sponsored by
About this trial
This is an interventional treatment trial for Tethered Cord Syndrome
Eligibility Criteria
Inclusion Criteria:
- patients aged 14-20 years, without gender limitation, are willing to sign informed consent;
- patients diagnosed with tethered cord syndrome (TCS);
- patients accepted untethering surgery or resection of intra-lipomas or myelomeningocele after birth;
- patients present with the recent occurrence of bladder or bowel dysfunction, with progressive deterioration, may be accompanied by motor deficits of lower extremity;
- urodynamic examination suggests neurogenic injury;
- the current conventional treatment is difficult to achieve satisfactory clinical outcomes.
Exclusion Criteria:
- bladder or ureter obstruction;
- other types of neurogenic bladder dysfunction (spinal cord injury, cerebral palsy, other brain injuries);
- anorectal malformations;
- poor health condition, unable to tolerate surgery;
- patients (or their guardians) cannot give full informed consent for cognitive dysfunction;
- patients who have participated in other clinical trials in the past 1 month.
- patients with active hepatitis B (including HBeAg) or serological markers (HBsAg or / and HBeAg or / and HBcAb), hepatitis C, tuberculosis, cytomegalovirus infection, severe fungal infection or HIV infection;
- patients with active peptic ulcers within 3 months before randomization.
- patients with malignant neoplasms
Sites / Locations
- Shanghai Changzheng HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Conservative treatment
Capsule surgery
Arm Description
Conservative physiotherapy, intermittent catheterization, or drug treatment for bladder or bowel dysfunction
Nerve root axial decompression surgery (Capsule surgery)
Outcomes
Primary Outcome Measures
Changes of patient-reported scores assessing bladder function
International Consultation on Incontinence Modular Questionnaire Short Version (ICI-Q-SF) is used to assess urinary function and the impacts on patient's quality of life due to urinary problems.
Secondary Outcome Measures
Changes of patient-reported scores assessing bowel function
Rintala Score is applied to assess bowel function and its effects on patients' quality of life.
Changes of patient-reported quality of life due to bladder dysfuction
A new developed Chinese version of questionnaire is used to assess the quality of life in patients and parents due to bladder dysfunction.
Bladder function
Urodynamic testing is performed to determine the bladder function, including bladder pressure, bladder capacity, residual volume, and compliance of bladder.
Muscle power
Muscle power is tested by manual assessment, which is classified into 6 levels.
Improvment of clubfoot deformity
Pirani questionnaire is applied to assess the severity of clubfoot deformity by the examiner.
Changes of patient-reported scores assessing foot deformity
Foot function index is applied to assess the impacts on patients' quality of life due to foot deformity
Changes of patient-reported scores assessing function of back and lower limbs
Oswestry disability index (ODI) is applied to assess the function of back and lower limbs.
Changes of patient-reported quality of life
SF-12 is applied to assess the impacts on quality of life due to tethered cord syndrome.
Full Information
NCT ID
NCT03262844
First Posted
August 6, 2017
Last Updated
September 26, 2018
Sponsor
Shanghai Changzheng Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03262844
Brief Title
Efficacy and Safety of Nerve Root Axial Decompression Surgery in The Treatment of Tethered Cord Syndrome
Official Title
Efficacy and Safety of Nerve Root Axial Decompression Surgery in The Treatment of Tethered Cord Syndrome: A Conservative Treatment- Controlled, Randomized, Clinical Study
Study Type
Interventional
2. Study Status
Record Verification Date
September 2018
Overall Recruitment Status
Unknown status
Study Start Date
June 16, 2017 (Actual)
Primary Completion Date
April 2019 (Anticipated)
Study Completion Date
April 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Changzheng Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Background: Tethered cord syndrome (TCS) is a progressive clinical condition including a series of neurological dysfunctions and deformities attributable to abnormally increased tension on the spinal cord, which is lacking effective treatment to relieve the symptoms and prevent progression. Dr. Shi recently proposed a new technique as nerve root axial decompression surgery, which is also called capsule surgery, to treat patients with TCS. Yet, the effectiveness and safety should be further studied.
Purpose: The aim of this study is to compare the effectiveness and safety of clinical outcomes between capsule surgery and conservative treatment in patients with TCS. A study hypothesis is that outcomes will be improved after capsule surgery.
Methods: This study is a randomized clinical trial with a two-factor (2x7) research design. The TCS patients will be randomly assigned in one of the two treatment groups: capsule surgery and conservative treatment. Seven outcome measures will be collected pre-operative for baseline, and then at1, 12, 24, 48, and 96 weeks post-operative follow-up visits, including: International Consultation on Incontinence Modular Questionnaire Short Version (ICI-Q-SF), Rintala Score, a new developed Chinese version of questionnaire, Oswestry disability index (ODI), SF-12, foot function index (FFI) and Pirani score. Urodynamic testing, bladder ultrasonography, electromyogram, muscle strength and sensation of lower limbs will be obtained before and post treatment, to determine the patient's function of lower limbs. The investigator performing the outcome measures will be blinded to group assignment, and therefore will not participate in treatment. After randomization, the conservative group will be followed up in the outpatient clinic. The capsule surgery group will receive the nerve root axial decompression surgery (capsule surgery).
Data Analysis: Two 2x7 MANOVAs with repeated measures will be used to examine the differences in the seven measures between groups and at the five different time frames with the α level set at 0.05. Non-parametric tests (Mann-Whitney U tests) will be used to compare the differences in the urodynamics and muscle strength data over time and between groups.
Detailed Description
Background: Tethered cord syndrome (TCS) is a progressive clinical condition including a series of neurological dysfunctions and deformities attributable to abnormally increased tension on the spinal cord. The standard surgical treatment is untethering the spinal cord and correction of the related deformity. Although reported results are encouraging, it continues to pose challenges on management of TCS patients. Symptomatic re-tethering seems to be an inevitable result, which occurs in 20%-50% patients after untethering. Recently, filum dissection was found no good to improve urinary symptoms compared to conservative treatment in teenagers as reported in an RCT study. Also, it remained controversy when to perform the surgery and how to evaluate the benefits of surgery or conservative treatment. Dr. Shi recently proposed a new technique as nerve root axial decompression surgery, which is also called capsule surgery, to treat patients with TCS. Yet, the effectiveness and safety should be further studied.
Purpose: The aim of this study is to compare the effectiveness and safety of clinical outcomes between capsule surgery and conservative treatment in patients with TCS. A study hypothesis is that outcomes will be improved after capsule surgery.
Methods: This study is a randomized clinical trial with a two-factor (2x7) research design. The TCS patients will be randomly assigned in one of the two treatment groups: capsule surgery and conservative treatment. Seven outcome measures will be collected pre-operative for baseline, and then at1, 12, 24, 48, and 96 weeks post-operative follow-up visits, including: (1) International Consultation on Incontinence Modular Questionnaire Short Version (ICI-Q-SF) to assess the urinary functions, (2) Rintala Score for bowel function, (3) a new developed Chinese version of questionnaire to assess the quality of life in patients and parents due to bladder dysfunction. (4) Oswestry disability index (ODI) to assess the function of back and lower limbs, (5)SF-12 for whole quality of life, (6) Pirani score to assess clubfoot deformity, and (7) foot function index to assess the impacts on quality of life due to clubfoot. Urodynamics, bladder ultrasonography, muscle strength and sensation of lower limbs will be obtained before and post treatment, to determine the patient's function of lower limbs. The investigator performing the outcome measures will be blinded to group assignment, and therefore will not participate in treatment. After randomization, the conservative group will be followed up in the outpatient clinic. The capsule surgery group will receive the nerve root axial decompression surgery.
Data Analysis: Two 2x7 MANOVAs with repeated measures will be used to examine the differences in the four measures between groups and at the five different time frames with the α level set at 0.05. Non-parametric tests (Mann-Whitney U tests) will be used to compare the differences in the urodynamics and muscle strength data over time and between groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tethered Cord Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The statistical analysist do not know the group assignment.
Allocation
Randomized
Enrollment
36 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Conservative treatment
Arm Type
Placebo Comparator
Arm Description
Conservative physiotherapy, intermittent catheterization, or drug treatment for bladder or bowel dysfunction
Arm Title
Capsule surgery
Arm Type
Experimental
Arm Description
Nerve root axial decompression surgery (Capsule surgery)
Intervention Type
Behavioral
Intervention Name(s)
Conservative treatment
Intervention Description
The conservative treatment group will be given diet and nursing guidance, then the drug treatment or physiotherapy will be given according to the conditions of patients. Patients with bladder dysfunction will be guided to perform routine intermittent catheterization with help of their parents.
Intervention Type
Procedure
Intervention Name(s)
Capsule surgery
Intervention Description
In the multiple segments of the spine, articular facet joint and intervertebral disc will be resected to achieve the effect of decompression.
Specific surgical segments, osteotomy range, decompression degree of each patient needs to be designed individually.
Primary Outcome Measure Information:
Title
Changes of patient-reported scores assessing bladder function
Description
International Consultation on Incontinence Modular Questionnaire Short Version (ICI-Q-SF) is used to assess urinary function and the impacts on patient's quality of life due to urinary problems.
Time Frame
At 1 week pre- and 1, 12, 24, 48, and 96 weeks post-operative follow-up visits.
Secondary Outcome Measure Information:
Title
Changes of patient-reported scores assessing bowel function
Description
Rintala Score is applied to assess bowel function and its effects on patients' quality of life.
Time Frame
At 1 week pre- and 1, 12, 24, 48, and 96 weeks post-operative follow-up visits.
Title
Changes of patient-reported quality of life due to bladder dysfuction
Description
A new developed Chinese version of questionnaire is used to assess the quality of life in patients and parents due to bladder dysfunction.
Time Frame
At 1 week pre- and 1, 12, 24, 48, and 96 weeks post-operative follow-up visits.
Title
Bladder function
Description
Urodynamic testing is performed to determine the bladder function, including bladder pressure, bladder capacity, residual volume, and compliance of bladder.
Time Frame
At 1 week pre- and 1, 12, 48, and 96 weeks post-operative follow-up visits.
Title
Muscle power
Description
Muscle power is tested by manual assessment, which is classified into 6 levels.
Time Frame
At 1 week pre- and 1, 12, 24, 48, and 96 weeks post-operative follow-up visits.
Title
Improvment of clubfoot deformity
Description
Pirani questionnaire is applied to assess the severity of clubfoot deformity by the examiner.
Time Frame
At 1 week pre- and 1, 12, 24, 48, and 96 weeks post-operative follow-up visits.
Title
Changes of patient-reported scores assessing foot deformity
Description
Foot function index is applied to assess the impacts on patients' quality of life due to foot deformity
Time Frame
At 1 week pre- and 1, 12, 24, 48, and 96 weeks post-operative follow-up visits.
Title
Changes of patient-reported scores assessing function of back and lower limbs
Description
Oswestry disability index (ODI) is applied to assess the function of back and lower limbs.
Time Frame
At 1 week pre- and 1, 12, 24, 48, and 96 weeks post-operative follow-up visits.
Title
Changes of patient-reported quality of life
Description
SF-12 is applied to assess the impacts on quality of life due to tethered cord syndrome.
Time Frame
At 1 week pre- and 1, 12, 24, 48, and 96 weeks post-operative follow-up visits.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients aged 14-20 years, without gender limitation, are willing to sign informed consent;
patients diagnosed with tethered cord syndrome (TCS);
patients accepted untethering surgery or resection of intra-lipomas or myelomeningocele after birth;
patients present with the recent occurrence of bladder or bowel dysfunction, with progressive deterioration, may be accompanied by motor deficits of lower extremity;
urodynamic examination suggests neurogenic injury;
the current conventional treatment is difficult to achieve satisfactory clinical outcomes.
Exclusion Criteria:
bladder or ureter obstruction;
other types of neurogenic bladder dysfunction (spinal cord injury, cerebral palsy, other brain injuries);
anorectal malformations;
poor health condition, unable to tolerate surgery;
patients (or their guardians) cannot give full informed consent for cognitive dysfunction;
patients who have participated in other clinical trials in the past 1 month.
patients with active hepatitis B (including HBeAg) or serological markers (HBsAg or / and HBeAg or / and HBcAb), hepatitis C, tuberculosis, cytomegalovirus infection, severe fungal infection or HIV infection;
patients with active peptic ulcers within 3 months before randomization.
patients with malignant neoplasms
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ximing Xu, MD
Phone
+8618801784094
Email
xi_mingxu@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiangang Shi, MD
Organizational Affiliation
Shanghai Changzheng Hospital, Second Military Medical University
Official's Role
Study Chair
Facility Information:
Facility Name
Shanghai Changzheng Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ximing Xu, MD
Phone
18801784094
Email
xi_mingxu@hotmail.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
26926544
Citation
Steinbok P, MacNeily AE, Hengel AR, Afshar K, Landgraf JM, Hader W, Pugh J. Filum Section for Urinary Incontinence in Children with Occult Tethered Cord Syndrome: A Randomized, Controlled Pilot Study. J Urol. 2016 Apr;195(4 Pt 2):1183-8. doi: 10.1016/j.juro.2015.09.082. Epub 2016 Feb 28.
Results Reference
background
Learn more about this trial
Efficacy and Safety of Nerve Root Axial Decompression Surgery in The Treatment of Tethered Cord Syndrome
We'll reach out to this number within 24 hrs