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Trial · NCT07537816

Effects of Vadadustat on Anemia, Quality of Life, and Inflammation in Dialysis Patients

NCT07537816, Phase 4, Not yet recruiting, Mackay Memorial Hospital

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effects of Vadadustat on Anemia, Quality of Life, and Inflammation in Dialysis Patients. Trials, record NCT07537816. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07537816

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Effects of Vadadustat on Anemia, Quality of Life, and Inflammation in Dialysis Patients
NCT number
NCT07537816
Status
Not yet recruiting
Phases
Phase 4
Enrollment
40 participants, estimated
Lead sponsor
Mackay Memorial Hospital
Conditions
Renal Anemia
Interventions
Vadadustat
First posted
2026-04-17
Last updated
2026-04-23

Source ClinicalTrials.gov

Registered outcomes10

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

ListOutcomeTime frameDescription
PrimaryChange in HemoglobinBaseline and end of each 8-week treatment period (up to 5 months).
Within-participant change in hemoglobin during add-on vadadustat treatment compared with background darbepoetin alfa alone in this two-period, two-sequence crossover study in patients receiving maintenance peritoneal dialysis.
SecondaryChange in SF-36 Physical Component Summary scoreBaseline and end of each 8-week treatment period (up to 5 months).
Change in health-related quality of life as assessed by the 36-Item Short Form Health Survey (SF-36) Physical Component Summary (PCS) score during add-on vadadustat treatment compared with background darbepoetin alfa alone in this two-period, two-sequence crossover study in patients receiving maintenance peritoneal dialysis. Higher scores indicate better physical health status.
SecondaryChange in SF-36 Mental Component Summary scoreBaseline and end of each 8-week treatment period (up to 5 months).
Change in health-related quality of life as assessed by the 36-Item Short Form Health Survey (SF-36) Mental Component Summary (MCS) score during add-on vadadustat treatment compared with background darbepoetin alfa alone in this two-period, two-sequence crossover study in patients receiving maintenance peritoneal dialysis. Higher scores indicate better mental health status.
SecondaryChange in C-reactive proteinBaseline and monthly during the study period, up to 5 months.Change in serum C-reactive protein during add-on vadadustat treatment compared with background darbepoetin alfa alone.
SecondaryChange in erythrocyte sedimentation rateBaseline and monthly during the study period, up to 5 months.Change in erythrocyte sedimentation rate during add-on vadadustat treatment compared with background darbepoetin alfa alone.
SecondaryChange in interleukin-6Baseline and monthly during the study period, up to 5 months.Change in serum interleukin-6 during add-on vadadustat treatment compared with background darbepoetin alfa alone.
SecondaryChange in serum ironBaseline and monthly during the study period, up to 5 months.Change in serum iron during add-on vadadustat treatment compared with background darbepoetin alfa alone.
SecondaryChange in total iron-binding capacityBaseline and monthly during the study period, up to 5 months.Change in serum total iron-binding capacity during add-on vadadustat treatment compared with background darbepoetin alfa alone.
SecondaryChange in ferritinBaseline and monthly during the study period, up to 5 months.Change in serum ferritin during add-on vadadustat treatment compared with background darbepoetin alfa alone.
SecondaryChange in transferrin saturationBaseline and monthly during the study period, up to 5 months.Change in transferrin saturation during add-on vadadustat treatment compared with background darbepoetin alfa alone.

Outcomes0

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

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07537816

GET https://conductscience.org/api/trials/v1/NCT07537816/registered