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Hyperbaric Oxygen and Orthopedic Comprehensive Treatment for Traumatic Incomplete Spinal Cord Injury in the Plateau

Primary Purpose

Spinal Cord Injuries

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
control group
hyperbaric oxygen group
Sponsored by
Qinghai University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Cord Injuries

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Incomplete spinal cord injury (SCI) (contusion) assessed by rectal examination in accordance with International standards for neurological classification of spinal cord injury (Revised 2011);
  • SCI revealed by CT, X-ray or MRI scan;
  • Clear trauma in the spine;
  • Different degrees of movement, sensation and sphincter dysfunction below spine injury segment;
  • Living in the plateau for at least 2 years;
  • Age of ≥18 years, irrespective of sex.

Exclusion Criteria:

  • Brain trauma, combined injury of chest and abdominal organs, instable vital signs or disturbance of consciousness;
  • Coagulation dysfunction;
  • Hypertension, heart disease, diabetes, stroke, brain damage and neurological disease;
  • Lumbar surgery, trauma history, lumbar fracture, infection, tumor, severe osteoporosis;
  • Nerve pain, limb cramps, periarticular heterotopic ossification;
  • Other diseases that may impact neurological examination;
  • Participating in other clinical trials.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    control group

    hyperbaric oxygen group

    Arm Description

    Patients with traumatic incomplete spinal cord injury (SCI) in the control group are treated with pedicle screw fixation and decompressive laminectomy.

    Patients with traumatic incomplete spinal cord injury (SCI) in the hyperbaric oxygen group are treated with pedicle screw fixation and decompressive laminectomy, and are given 0.2 MPa hyperbaric oxygen (HBO), once a day, 10 times as a course, with 5-7 days of resting between two courses, totally four courses.

    Outcomes

    Primary Outcome Measures

    Modified Barthel index
    To assess the difference before and after treatment

    Secondary Outcome Measures

    American Spinal Injury Association impairment scale grading
    To assess the recovery of spine nerve function before and after treatment. American Spinal Injury Association(ASIA) is a spinal cord injury (SCI) neurological assessment criteria developed by the American Spinal Injury Association in 1982, contains grades A-E.

    Full Information

    First Posted
    April 8, 2017
    Last Updated
    February 7, 2018
    Sponsor
    Qinghai University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03112941
    Brief Title
    Hyperbaric Oxygen and Orthopedic Comprehensive Treatment for Traumatic Incomplete Spinal Cord Injury in the Plateau
    Official Title
    Hyperbaric Oxygen and Orthopedic Comprehensive Treatment for Traumatic Incomplete Spinal Cord Injury in the Plateau: an Open-label Randomized Controlled Clinical Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2012 (Actual)
    Primary Completion Date
    June 2016 (Actual)
    Study Completion Date
    December 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Qinghai University

    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
    To observe modified Barthel index, American Spinal Injury Association (ASIA) impairment scale grading, sensory score and motor score in patients with incomplete SCI in the plateau using 0.2 MPa HBO combined with pedicle screw fixation and decompressive laminectomy so as to investigate the effect of HBO therapy on incomplete SCI in the plateau.
    Detailed Description
    History and current related studies Spinal cord injury (SCI) is a kind of serious disabling disease caused by various factors (such as trauma, infection), and can lead to paralysis. At present, 16-40 people/million suffer from SCI in developed countries every year; 34.3-60 people affect SCI in China every year. SCI is often caused by physical trauma, such as rotation, compression and hyperextension. This type of SCI is also known as traumatic spinal cord injury (TSCI). At present, there are many treatments for TSCI, but the prognosis is poor. Hyperbaric oxygen (HBO) therapy is the medical use of oxygen at a level higher than atmospheric pressure for treating hypoxic disease (Hu et al., 2016). Secondary injuries, such as edema, neuronal necrosis, blood and spinal cord barrier disorders, have been shown to be strongly associated with a large number of inflammatory factors. HBO can effectively inhibit the generation of inflammatory factors, and promote repair and regeneration of neurons. Moreover, HBO can relieve hypoxia, protect the surrounding tissue, reduce the mitochondrial dysfunction in injury area, reduce bleeding area and reduce edema. HBO has been used to treat TSCI for a long time. Holbach et al. first found that HBO therapy improved postoperative dysfunction in TSCI patients. In recent years, a number of clinical studies have focused on HBO therapy for TSCI, and the patients recovered well. Atmospheric pressure is very low in the plateau, and oxygen content in plateau environment is less than that in plain area. Secondary apoptosis induced by ischemia and hypoxia after SCI is the main cause of spinal cord dysfunction. HBO therapy can increase the dissolved oxygen, which is helpful for the recovery of incomplete spinal nerve function. Therefore, HBO therapy has higher therapeutic value in plateau than in plain. Data management The observation forms were filled out accurately, completely and timely by researchers. Data were recorded electronically by data managers using a double-data entry strategy. The electronic database was collated and locked only by the project manager. The locked electronic database could not be altered. All data regarding this trial were preserved by the Affiliated Hospital of Qinghai University, China. The electronic database was statistically analyzed by a professional statistician. Anonymized trial data will be published at www.figshare.com. Statistical analysis Statistical analysis was performed using SPSS 22.0 software (IBM, Armonk, NY, USA). Measurement data were expressed as mean ± SD. Normality test and variance homogeneity test were conducted. Normally distributed data with homogeneity were compared using one-way analysis of variance. Non-normally distributed data were compared using Wilcoxon two-sample rank sum test. Ranked data were analyzed using rank sum test. A value of P < 0.05 was considered statistically significant. Results followed the intention-to-treat principle. Confidentiality Identifying information, such as observation forms and informed consent, was password-protected and not altered for future reference. No person, other than an authorized researcher, may be in contact with it.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Spinal Cord Injuries

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    164 patients with traumatic incomplete spinal cord injury (SCI) were recruited in the plateau from June 2012 to February 2016.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    164 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    control group
    Arm Type
    Experimental
    Arm Description
    Patients with traumatic incomplete spinal cord injury (SCI) in the control group are treated with pedicle screw fixation and decompressive laminectomy.
    Arm Title
    hyperbaric oxygen group
    Arm Type
    Experimental
    Arm Description
    Patients with traumatic incomplete spinal cord injury (SCI) in the hyperbaric oxygen group are treated with pedicle screw fixation and decompressive laminectomy, and are given 0.2 MPa hyperbaric oxygen (HBO), once a day, 10 times as a course, with 5-7 days of resting between two courses, totally four courses.
    Intervention Type
    Procedure
    Intervention Name(s)
    control group
    Intervention Description
    Patients with traumatic incomplete spinal cord injury (SCI) in the control group are treated with pedicle screw fixation and decompressive laminectomy.
    Intervention Type
    Other
    Intervention Name(s)
    hyperbaric oxygen group
    Intervention Description
    Patients with traumatic incomplete spinal cord injury (SCI) in the hyperbaric oxygen group are treated with pedicle screw fixation and decompressive laminectomy, and are given 0.2 MPa hyperbaric oxygen (HBO), once a day, 10 times as a course, with 5-7 days of resting between two courses, totally four courses.
    Primary Outcome Measure Information:
    Title
    Modified Barthel index
    Description
    To assess the difference before and after treatment
    Time Frame
    40 days after treatment
    Secondary Outcome Measure Information:
    Title
    American Spinal Injury Association impairment scale grading
    Description
    To assess the recovery of spine nerve function before and after treatment. American Spinal Injury Association(ASIA) is a spinal cord injury (SCI) neurological assessment criteria developed by the American Spinal Injury Association in 1982, contains grades A-E.
    Time Frame
    40 days after treatment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Incomplete spinal cord injury (SCI) (contusion) assessed by rectal examination in accordance with International standards for neurological classification of spinal cord injury (Revised 2011); SCI revealed by CT, X-ray or MRI scan; Clear trauma in the spine; Different degrees of movement, sensation and sphincter dysfunction below spine injury segment; Living in the plateau for at least 2 years; Age of ≥18 years, irrespective of sex. Exclusion Criteria: Brain trauma, combined injury of chest and abdominal organs, instable vital signs or disturbance of consciousness; Coagulation dysfunction; Hypertension, heart disease, diabetes, stroke, brain damage and neurological disease; Lumbar surgery, trauma history, lumbar fracture, infection, tumor, severe osteoporosis; Nerve pain, limb cramps, periarticular heterotopic ossification; Other diseases that may impact neurological examination; Participating in other clinical trials.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jun Ma, Ph.D
    Organizational Affiliation
    Affiliated Hospital of Qinghai University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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    Hyperbaric Oxygen and Orthopedic Comprehensive Treatment for Traumatic Incomplete Spinal Cord Injury in the Plateau

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