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NCT Number: NCT05653206

Incomplete Cervical SCI Without Instability

A multicenter, international, prospective, observational case series patient cohort with incomplete cervical SCI without instability will be enrolled to obtain information and data that could inform the feasibility of administering a set of additional core and optional outcome assessments in cervical SCI patients to capture the aspects of neurologic impairment. Baseline, intraoperative, and postoperative characteristics, including demographics, injury details, treatment details, neurological assessments, gait and balance assessments and upper extremity assessments, will be recorded for adult patients.

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Instituto de Ortopedia E Traumatologia Do Hospital Das Clinicas Da Universidade de Sao Paulo, São Paulo, Brazil

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About this study

This prospective multicenter study will enroll 50 adult patients with acute traumatic cervical SCI with ISNCSCI AIS Grade D or sensory deficits only without biomechanical instability.

Patients will be assessed at the baseline visit and subsequently be followed up at 3 and 6 months. All decisions regarding the treatment and clinical management will be left to the attending spinal surgeon and will follow the local standard of care.

The core outcome assessments include:

  • Neurological status by the ISNCSCI
  • Patient-reported outcome measures (PROMs) of Short Form-36 (SF-36) v2 and Neuropathic Pain Scale (NPS)
  • The Spinal Cord Independence Measure (SCIM) v3
  • Gait and balance evaluated using the ten-meter walk test (10mWT) and Walking Index for Spinal Cord Injury (WISCI) v2
  • Upper extremity impairment evaluated using the grip strength with digital dynamometry, pinch strength (key pinch and tip-to-tip pinch), and the Partial Graded Redefined Assessment of Strength Sensibility and Prehension (GRASSP) v2.

All core outcome assessments will be performed at the baseline, 3-, and 6-month visits except for the PROMs, SCIM v3, key pinch and tip-to-tip pinch, which will be assessed only at the 3- and 6-month visits.

The optional outcome assessment is the multiparametric quantitative spinal cord magnetic resonance imaging (MRI)/diffusion tensor imaging (DTI) which will be performed at baseline, 3-, and 6-month visits if it is done at the surgeon's discretion.

The goal of this study is to obtain information and data that could inform the feasibility of administering a set of additional core and optional outcome assessments in cervical SCI patients with incomplete tetraplegia without spinal instability to capture the aspects of neurologic impairment that may not be well represented in the ISNCSCI examination.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-80 years, inclusive
  • Diagnosis of acute traumatic cervical SCI with ISNCSCI AIS Grade D or sensory deficits only within 92 hours post injury
  • Cervical neurological level of injury (C2-C8)
  • MRI, using any imaging protocols (conventional, multiparametric, or quantitative), taken according to standard of care
  • Presence of spinal cord compression on the MRI
  • Absence of biomechanical instability to the extent that would mandate stabilization surgery by the treating surgeon
  • Ability to provide informed consent according to the IRB/EC defined and approved procedures

Exclusion criteria

  • Nontraumatic SCI
  • Concomitant traumatic brain injury or polytrauma that could preclude accurate or reliable assessments of the outcome assessments
  • Uncontrolled severe systemic diseases, preexisting neurological, musculoskeletal, or general medical conditions which could preclude accurate assessments or FUs
  • Individuals unable to undergo MRI

Treatment and study plan

Nonsurgical treatment

Procedure

Cervical collar, Halo ring, Halo vest, cervical braces, skeletal skull traction, MAP, steroids, observation or bedrest

surgical treatment

Procedure

Anterior discectomy and instrumented fusion (single level), Anterior discectomy and instrumented fusion (multi-level), Posterior decompression-laminectomy, Posterior decompression-laminoplasty, Posterior decompression and instrumented fusion, Combined anterior and posterior decompression and instrumented fusion

Primary outcomes

  1. The proportion of the core outcome assessments successfully completed at each visit

    Time frame: up to 6 months

    For baseline and each FU visit, the completion status of each core outcome assessment

  2. Time required to complete the individual core outcome assessments

    Time frame: up to 6 months

    For baseline and each FU visit, the time required for completion for each core outcome assessment will be recorded (start time, end time, and duration in mins)

  3. Total time required to complete all core outcome assessments at each visit

    Time frame: up to 6 months

    The time required for completion will be measured to the nearest 0.1 second by using a digital timer, and the timing should start at the start of giving instructions to the patients or explaining the tests to the patients (start time) and end when the final score of the test is obtained (end time).

  4. Completion rate of individual core outcome assessments (and their scorings if applicable)

    Time frame: up to 6 months

    Completion rate of individual core outcome assessments at each visit.

  5. Completion rate of the multiparametric quantitative spinal cord MRI/DTI

    Time frame: up to 6 months

    Completion rate of the multiparametric quantitative spinal cord MRI/DTI

  6. FU visit compliance rate and reasons for non-compliance

    Time frame: up to 6 months

    Completion status of FU visits, recorded at 3- and 6-month visits

  7. Patient accrual rate

    Time frame: up to 6 months

    Whether the patient drops out from the study, recorded at the time of dropout

Secondary outcomes

  1. Results from the core outcome assessment ISNCSCI

    Time frame: up to 6 months

    Motor and sensory scores (motor score 0-100, pin prick score 0-112), AIS Grades, Clinical syndrome (Central Cord/Brown-Sequard/Anterior Cord/Conus Medullaris/Cauda Equina/No clinical syndrome/Not assessed)

  2. Results from the core outcome assessment SF-36 v2

    Time frame: up to 6 months

    Eight scale scores (0-100): physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, general mental health, social functioning, energy/fatigue or vitality, and general health perceptions

  3. Results from the core outcome assessment Neuropathic pain score

    Time frame: up to 6 months

    Score 0-100

  4. Results from the core outcome assessment SCIMv3

    Time frame: up to 6 months

    Three subscales: Self-care (0-20), Respiration and Sphincter Management (0-40), Mobility (room and toilet, 0-40)

  5. Results from the core outcome assessment WISCI v2

    Time frame: up to 6 months

    Level of walking (score 0-20)

  6. Results from the core outcome assessment Key pinch and tip-to-tip pinch

    Time frame: up to 6 months

    Pinch strength in kg

  7. Results from the core outcome assessment GRASSP v2

    Time frame: up to 6 months

    Eight subtest scores Strength (0-50), Palmar sensation (0-12), Prehension Ability (0-12), Prehension Performance (0-20)

Sponsors and collaborators

Lead sponsor

AO Foundation, AO Spine

Other

Registry information

Official study title

IN-TWIN: Traumatic Incomplete Tetraplegia Without Instability: a Prospective Multicenter Feasibility Study of Outcomes and Prognosis

Important dates

Study start
2023
Primary completion
2026
Study completion
2027
First posted
Dec 16, 2022
Registry last updated
Feb 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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