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Trial · NCT05650229

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in-patient-reported fatigue symptoms and impacts on daily living measured by Patient-Reported Outcomes Measurement Information System (PROMIS®) Fatigue PMD Short FormBaseline and 48 WeeksChange in t-score. Higher scores indicate greater fatigue severity.
PrimaryChange in 30 Second Site-to-Stand Test.Baseline and 48 WeeksChange in number of stands
SecondaryChange in Quality of Life in Neurological Disorders (Neuro-QoL) Lower Extremity Function (Mobility) Short FormBaseline and 48 weeksChange in t-score. Higher scores indicate greater functional ability.
SecondaryChange in Individual Activity Assessments - InterferenceBaseline and 48 Weeks
Assessing how much Primary Mitochondrial Disease symptoms get in the way of the ability to perform individually selected activities. A 5 point scale ranging from "No interference" to "Completely interferes"
SecondaryIndividual Activity Assessment - Change48 weeksAssessing the ability to perform individually selected activities compared to baseline. A 5 point scale ranging from "Much worse" to "Much better"
SecondaryChange in Patient Global Impression of SeverityBaseline and 48 weeksScale ranging from 1 (none) to 4 (severe).
SecondaryScore on Patient Global Impression of Change48 weeksScale ranging from 2 (much better) to -2 (much worse).
SecondaryChange in Clinician Global Impression of SeverityBaseline and 48 weeksScale ranging from 1 (none) to 4 (severe).
SecondaryScore on Clinician Global Impression of Change48 weeksScale ranging from 2 (much better) to -2 (much worse).
SecondaryChange in Newcastle Mitochondrial Disease Adult Scale (NMDAS) - subscales I-IIIBaseline and 48 weeksMeasured on a 6-point rating scale from 0 to 5. Total score across all 3 subscales ranges from 0 to 140. Higher scores indicate more extensive and severe system involvements.
SecondaryChange from baseline in Glycated haemoglobin (HbA1c) for subjects with diabetesBaseline and 48 weeksmmol/mol

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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GET https://conductscience.org/api/trials/v1/NCT05650229/registered