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Trial · NCT02974114

Outcomes12

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Pain Free State (Day 3) in Error Adjusted Simple Reaction Time (SRT) in the Pain State (Day 2)At Day 2 (pre and post-treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
milliseconds (msec)MEDIAN
PRIMARYChange From Pain-free State (Day 3) in Reaction Time in the Pain State (Day 2)At Day 2 (pre and post-treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
msecMEDIAN
PRIMARYChange From Pain-free State (Day 3) in Number of One Touch Stockings (OTS) of Cambridge Assessment Problems (on Which the First Box Choice Made Was Correct) in the Pain State (Day 2)At Day 2 (pre and post treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
OTS of correct first box choiceMEAN
PRIMARYChange From Pain-free State (Day 3) in Attention Switching Task (AST) Congruency Cost in the Pain State (Day 2)At Day 2 (pre and post treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
msecMEDIAN
PRIMARYChange From Pain-free State (Day 3) in Spatial Working Memory (SWM) Between Errors in the Pain State (Day 2)At Day 2 (pre and post treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
SWM between errorsMEAN
PRIMARYChange From Pain-free State (Day 3) in Rapid Visual Information Processing A Prime (RVPA) in the Pain State (Day 2)At Day 2 (pre and post treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
msecMEDIAN
SECONDARYChange From Pain-free State (Day 3) in Grip Force in Pain State (Day 2)At Day 2 (pre and post-treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
Kilogram (Kg)MEAN
SECONDARYChange From Pain-free State (Day 3) in Time to Standing in Pain State (Day 2)At Day 2 (pre and post treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
SecondsMEDIAN
SECONDARYChange From Pain-free State (Day 3) in Ground Reaction Force (GRF) in Pain State (Day 2)At Day 2 (pre and post treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
NewtonsMEAN
SECONDARYChange From Pain-free State (Day 3) in Contact Phase in Pain State (Day 2)At Day 2 (pre and post treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
SecondsMEDIAN
SECONDARYChange From Pain-free State (Day 3) in Stride Length in Pain State (Day 2)At Day 2 (pre and post treatment) and Day 3 of the study
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
CentimeterMEAN
SECONDARYChange From Pain-free State (Day 3) in Walking Speed in Pain State (Day 2)At Day 2 (pre and post-treatment) and Day 3
Modified Intent-to-Treat (mITT, N=20) Population: All the participants who were randomized, received at least one dose of the study treatment and had at least one post-baseline assessment without any violation of study inclusion-exclusion criteria were included in the mITT population.
meters/secondMEAN

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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