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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05987150
Other study ID # 2021-398-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2022
Est. completion date April 30, 2023

Study information

Verified date August 2023
Source The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Spinal cord compression is commonly seen in patients with severe kyphosis. However, conventional morphologic magnetic resonance imaging (MRI) was unable to detect the damage in microstructural integrity of the spinal cord around the apical vertebrae in these patients. The aim of the study was to evaluate the neuronal metrics/microstructure of the spinal cord around apical region in patients with hyperkyphosis using diffusion tensor imaging (DTI).


Description:

Spinal cord compression is commonly seen in patients with severe kyphosis. However, conventional morphologic magnetic resonance imaging (MRI) was unable to detect the damage in microstructural integrity of the spinal cord around the apical vertebrae in these patients. The aim of the study was to evaluate the neuronal metrics/microstructure of the spinal cord around apical region in patients with hyperkyphosis using diffusion tensor imaging (DTI). Twenty-four patients with hyperkyphosis aged 46.1±22.8 years who underwent 3.0T MRI examination with DTI sequence were prospectively enrolled from July 2022 to January 2023. Patients were divided into three groups according to spinal cord/cerebrospinal fluid architecture (CSF) on sagittal-T2 MRI of the thoracic apex: Type A-circular cord with visible CSF, Type B-circular cord but no visible CSF at apical dorsal, and Type C-spinal cord deformed without intervening CSF. The Fractional Anisotropy (FA) values acquired from DTI were compared among different groups. Correlations between DTI parameters and global kyphosis (GK)/sagittal deformity angular ratio (SDAR) were evaluated using Pearson correlation coefficients.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date April 30, 2023
Est. primary completion date January 31, 2023
Accepts healthy volunteers No
Gender All
Age group 11 Years to 78 Years
Eligibility Inclusion Criteria: - diagnosis of hyperkyphosis; - the apex located at the thoracal region (T1-T12); - full DTI data; - records of detailed and systematic neurological physical examination. Exclusion Criteria: - any case with active infection, tumor, or trauma; - any cases of comorbidity of neurofibromatosis type I; - any cases combined with spinal syringomyelia, split cord malformations or diastematomyelia, tethered cord syndrome; - previous spinal surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
Variation in anisotropy of the Spinal Cord using diffusion tensor imaging
All examinations were performed on a 3.0-T MRI machine with a 12-channel spine special coil (Ingenia CX, Philips Healthcare, Best, the Netherlands). The multi-sequence MRI protocol included conventional T1-weighted (sag & tra), T2-weighted (sag & tra), and DTI sequence.

Locations

Country Name City State
China Drum Tower Hospital of Nanjing University Medical School Nanjing Jiang Su

Sponsors (1)

Lead Sponsor Collaborator
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fractional anisotropy (FA) values Raw DTI data were postprocessed on FuncTool (GE) software. After an initial correction of geometric distortions, the color-coded FA maps were generated. preoperative
Secondary Global kyphosis (GK) in degrees Measured on anteroposterior and lateral radiographs and defined as the angle from upper to lower most tilted end vertebrae. preoperative
Secondary Sagittal deformity angular ratio (SDAR) Divided GK by the number of levels spanning the curve. preoperative
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