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Study identifier: NCT06871254 Synced from ClinicalTrials.gov · August 11, 2026
● Study status: RecruitingSCINC

Spinal Cord Injury Neurorecovery Collaboration

Condition: Spinal Cord Injuries  ·  Sponsor: University of Melbourne

PhaseNA
Planned participants24
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
WhereHeidelberg, Victoria, Australia

Interested? Contact the study team ↓

For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

SCINC is an adaptive design Master protocol that seeks to determine if there is "sufficient promise" of beneficial effect of treatment combinations to enhance motor recovery in pre-specified strata of people with a spinal cord injury.

This description comes directly from the study's public registry record.

Talk to the study team

Laura Stendell  ·  (+61) 468 862 693  ·  laura.stendell@unimelb.edu.au

Nicole Sheers, PhD  ·  nsheers@unimelb.edu.au

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

SCINC Inclusion Criteria: \- Person with SCI SCINC Exclusion Criteria: \- Proven contraindication to intervention RRULI: Appendix 1 (TIH + ET) study-specific inclusion criteria: * Adults \> 18 years of age * Able to independently ventilate * Chronic SCI (\>1 years post-injury or impairment onset) * Tetraplegia (C2-T1 level of injury) * Evidence of motor incomplete paralysis in the upper limb below the neurological level of injury * Have a documented management plan for their AD if it occurs. RRULI: Appendix 1 (TIH + ET) study-specific exclusion criteria: * Pregnancy * Medical instability, including current or recent (within the previous 6 weeks) infection or inflammation * Current or recent (within the previous 6 weeks) pressure ulcers or cutaneous lesions * Poorly controlled diabetes * An episode of AD in the previous 6 months that required medical intervention to resolve * Significant other neurological, psychiatric, pulmonary, cardiovascular, orthopaedic, or oncological conditions. * Currently taking part in another clinical trial * Upper limb contracture

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Austin HealthHeidelberg, Victoria, AustraliaRecruiting

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Heidelberg

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