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What is the Preferred Angle of Traction to Decompress Cervical Nerve Roots?

Primary Purpose

Cervical Radiculopathy

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cervical Traction from different angles
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cervical Radiculopathy focused on measuring Traction, Decompression angles

Eligibility Criteria

20 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients will be included in the study if they have C5-C6 and C6-C7 paramedian disc protrusion manifested by unilateral symptoms in C6-C7 roots dermatome and myotomes of the upper extremities, second grade of disc bulge (2-3mm) which was detected from T2 axial view of MRI, and diagnosed as cervical disc protrusion (C5- C7) for at least three months.

Exclusion Criteria:

- Patients will be excluded from the study if they have upper cervical spine disc pathology, cord compression and upper motor neuron symptoms, curvature abnormalities of the neck including reversed curve (kyphotic) and deformities, cervical rib syndrome, double crush syndrome, diabetic neuropathy, text neck, short neck (churchill neck), marked facet joint, neuro-central joint arthropathic pathology, osteoporotic patients.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Active Comparator

    Active Comparator

    Arm Label

    traction therapy from neutral position

    traction therapy from lateral bending

    traction from flexion with lateral bending and rotation

    Arm Description

    Patients in this group will receive traction decompression from neutral neck position with rope angle (0°)

    patients will undergo traction decompression from (30°) lateral bending of the neck toward the non-affected side

    patients will be treated with traction decompression from (15°) neck flexion, (30°) lateral bending toward non- affected side and (15°) rotation to the affected side.

    Outcomes

    Primary Outcome Measures

    The Flexor Carpi radialis H-reflex
    The peak-to-peak amplitudes of four FCR-HR traces will be measured and averaged for each patient

    Secondary Outcome Measures

    Full Information

    First Posted
    March 30, 2019
    Last Updated
    March 30, 2019
    Sponsor
    Cairo University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03898739
    Brief Title
    What is the Preferred Angle of Traction to Decompress Cervical Nerve Roots?
    Official Title
    What is the Preferred Angle of Traction to Decompress Cervical Nerve Roots?
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    April 1, 2019 (Anticipated)
    Primary Completion Date
    August 1, 2019 (Anticipated)
    Study Completion Date
    September 1, 2019 (Anticipated)

    3. Sponsor/Collaborators

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

    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
    The purpose of the study is to investigate the effect of different angles of decompression on the Flexor Carpi Radialis (FCR) H-Reflex in patients with cervical radiculopathy
    Detailed Description
    Cervical traction has long been defined as a distracting force that separate the cervical segments and relieve nerve roots compression. Yet, there is lack of knowledge that reports the effects of different traction decompression angles and determines the proper angle of pull among different angles of decompression system

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cervical Radiculopathy
    Keywords
    Traction, Decompression angles

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    One independent variable with many levels.
    Masking
    ParticipantOutcomes Assessor
    Masking Description
    patients with cervical radiculopathy, caused by cervical paramedian disc protrusion at C5-C6 or C6-C7 levels will participate in the study. They will be assigned randomly into three equal groups; A, B and C.
    Allocation
    Randomized
    Enrollment
    45 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    traction therapy from neutral position
    Arm Type
    Active Comparator
    Arm Description
    Patients in this group will receive traction decompression from neutral neck position with rope angle (0°)
    Arm Title
    traction therapy from lateral bending
    Arm Type
    Active Comparator
    Arm Description
    patients will undergo traction decompression from (30°) lateral bending of the neck toward the non-affected side
    Arm Title
    traction from flexion with lateral bending and rotation
    Arm Type
    Active Comparator
    Arm Description
    patients will be treated with traction decompression from (15°) neck flexion, (30°) lateral bending toward non- affected side and (15°) rotation to the affected side.
    Intervention Type
    Other
    Intervention Name(s)
    Cervical Traction from different angles
    Intervention Description
    Intermittent traction will be applied, maximum force will be 16 kg, minimum force will be 12 kg, traction cycle of each minute consists of 20 seconds static traction at the maximum force then released down to the minimum force for 20 seconds then repeated for 20 seconds static traction. Traction session time will be 15 minutes, and the traction force will be increased progressively with speed (50%) of increment of force
    Primary Outcome Measure Information:
    Title
    The Flexor Carpi radialis H-reflex
    Description
    The peak-to-peak amplitudes of four FCR-HR traces will be measured and averaged for each patient
    Time Frame
    Changes from Baseline to 6-weeks after treatment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients will be included in the study if they have C5-C6 and C6-C7 paramedian disc protrusion manifested by unilateral symptoms in C6-C7 roots dermatome and myotomes of the upper extremities, second grade of disc bulge (2-3mm) which was detected from T2 axial view of MRI, and diagnosed as cervical disc protrusion (C5- C7) for at least three months. Exclusion Criteria: - Patients will be excluded from the study if they have upper cervical spine disc pathology, cord compression and upper motor neuron symptoms, curvature abnormalities of the neck including reversed curve (kyphotic) and deformities, cervical rib syndrome, double crush syndrome, diabetic neuropathy, text neck, short neck (churchill neck), marked facet joint, neuro-central joint arthropathic pathology, osteoporotic patients.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Abeer F Hanafy, PhD
    Phone
    01063044443
    Email
    abeerfarag22@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Mahmoud M Aly, Master
    Phone
    0237617691
    Email
    dr3mpt@yahoo.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Samiha H Hassan, Prof.
    Organizational Affiliation
    Professor of Physical Therapy for Neurology, Department of Physical Therapy for Neuromuscular Disorder and its Surgery, Faculty of Physical Therapy, Cairo University.
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Shaymaa M Abdelmeged, PhD
    Organizational Affiliation
    Lecturer at Department of Physical Therapy for Neuromuscular Disorder and its Surgery, Faculty of Physical Therapy, Cairo University.
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Salam M Elhafez, Prof.
    Organizational Affiliation
    Professor and Head of Department of Biomechanics, Faculty of Physical Therapy, Cairo University, Egypt
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    29492054
    Citation
    Khan RR, Awan WA, Rashid S, Masood T. A randomized controlled trial of intermittent Cervical Traction in sitting Vs. Supine position for the management of Cervical Radiculopathy. Pak J Med Sci. 2017 Nov-Dec;33(6):1333-1338. doi: 10.12669/pjms.336.13851.
    Results Reference
    background
    PubMed Identifier
    17697801
    Citation
    Liu J, Ebraheim NA, Sanford CG Jr, Patil V, Elsamaloty H, Treuhaft K, Farrell S. Quantitative changes in the cervical neural foramen resulting from axial traction: in vivo imaging study. Spine J. 2008 Jul-Aug;8(4):619-23. doi: 10.1016/j.spinee.2007.04.016. Epub 2007 Jun 21.
    Results Reference
    background

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