<p>Participant inclusion and exclusion criteria.</p>

Participant eligibility criteria for a two-phase clinical trial evaluating transcutaneous spinal cord stimulation (tSCS) for autonomic recovery in subacute spinal cord injury. The dataset, created by Ryo Nakahara and shared under CC-BY-4.0, was last updated in April 2026. It is a small 13.5 KB Excel file containing the inclusion and exclusion rules for a study targeting 26 adults with cervical or upper thoracic SCI.

Use Cases

• Assess recruitment feasibility for clinical trials based on the specific inclusion/exclusion criteria described.
• Analyze participant stratification for spinal cord injury studies based on injury level (≥T6) and AIS grade (A-C).
• Support meta-analysis of trial design by providing a concrete example of criteria for a subacute SCI neuromodulation study.
• Inform sample size planning for similar pilot studies based on the target enrollment of 26 participants.

Strengths

• Clear provenance from a registered clinical trial (NCT06540859) with ethics approval from the University of Washington IRB.
• Specific target population is defined: 26 adults with cervical or upper thoracic (≥T6) AIS A-C SCI within six months of injury.
• Study design details are provided, including a two-phase protocol with randomized and single-arm components.

Limitations

• Row count is unknown, which may limit suitability assessment.
• Column-level documentation is absent; field semantics must be inferred after download.
• The 13.5 KB size indicates a very limited scope, likely containing only criteria lists without patient-level data.

Provenance

Source

Clinical trial protocol authored by Ryo Nakahara, shared on figshare.

Collection Method

Defined as part of a clinical study design.

Time Range

Study targets individuals within six months since injury; dataset updated in 2026.

Freshness

Last updated 2026-04-20 17:37:18; freshness should be verified.

Geography

Likely based at the University of Washington, but specific participant geography is not stated.