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Trial · NCT05915286

Registered outcomes33

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

ListOutcomeTime frameDescription
PrimaryChange in 24-hour urine outputWeek 1Change in urine output measured from 24-hour urine collection.
PrimaryChange in 24-hour urine outputWeek 2Change in urine output measured from 24-hour urine collection.
PrimaryChange in 24-hour urine outputWeek 3Change in urine output measured from 24-hour urine collection.
PrimaryChange in 24-hour urine outputWeek 4Change in urine output measured from 24-hour urine collection.
PrimaryChange in 24-hour urine outputWeek 5Change in urine output measured from 24-hour urine collection.
PrimaryChange in residual renal functionWeek 1Calculated based on weekly bloodwork (urea and creatinine levels) and 24-hour urine collection.
PrimaryChange in residual renal functionWeek 2Calculated based on weekly bloodwork (urea and creatinine levels) and 24-hour urine collection.
PrimaryChange in residual renal functionWeek 3Calculated based on weekly bloodwork (urea and creatinine levels) and 24-hour urine collection.
PrimaryChange in residual renal functionWeek 4Calculated based on weekly bloodwork (urea and creatinine levels) and 24-hour urine collection.
PrimaryChange in residual renal functionWeek 5Calculated based on weekly bloodwork (urea and creatinine levels) and 24-hour urine collection.
SecondaryInterdialytic weight gainWeek 1Patient weight measured in kilograms
SecondaryInterdialytic weight gainWeek 2Patient weight measured in kilograms
SecondaryInterdialytic weight gainWeek 3Patient weight measured in kilograms
SecondaryInterdialytic weight gainWeek 4Patient weight measured in kilograms
SecondaryInterdialytic weight gainWeek 5Patient weight measured in kilograms
SecondaryPatient-reported outcomes - ESAS-rWeek 1Patient reported outcomes using the Edmonton Symptom Assessment System-revised (ESAS-r) questionnaire.
SecondaryPatient-reported outcomes - ESAS-rWeek 2Patient reported outcomes using the Edmonton Symptom Assessment System-revised (ESAS-r) questionnaire.
SecondaryPatient-reported outcomes - ESAS-rWeek 3Patient reported outcomes using the Edmonton Symptom Assessment System-revised (ESAS-r) questionnaire.
SecondaryPatient-reported outcomes - ESAS-rWeek 4Patient reported outcomes using the Edmonton Symptom Assessment System-revised (ESAS-r) questionnaire.
SecondaryPatient-reported outcomes - ESAS-rWeek 5Patient reported outcomes using the Edmonton Symptom Assessment System-revised (ESAS-r) questionnaire.

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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