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. 2022 Nov 1;8(6):e200034. doi: 10.1212/NXG.0000000000200034

Figure 1. CONSORT Diagram.

Figure 1

The safety analysis set included all randomized patients who received at least 1 dose (partial or complete) of the study drug. The mITT analysis set included all patients who took at least 1 dose (partial or complete) of the study drug and had at least 1 postbaseline spinal cord area segment C2-C3 measurement and SARA assessment at the same visit. The PP analysis set included all patients in the mITT analysis set who did not have a major protocol deviation. CONSORT = Consolidated Standards of Reporting Trials; mITT = modified intent-to-treat; PP = per protocol; SARA = Scale for the Assessment and Rating of Ataxia.