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Trial · NCT06226896

Effects of Dapagliflozin on Progression of Alport Syndrome

NCT06226896, Unknown, Nanjing University School of Medicine

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effects of Dapagliflozin on Progression of Alport Syndrome. Trials, record NCT06226896. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06226896

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Trial

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

Title
Effects of Dapagliflozin on Progression of Alport Syndrome
NCT number
NCT06226896
Status
Unknown
Enrollment
222 participants, actual
Lead sponsor
Nanjing University School of Medicine
Conditions
Alport Syndrome
Interventions
Dapagliflozin 10mg Tab
First posted
2024-01-26
Last updated
2024-09-05

Source ClinicalTrials.gov

Registered outcomes5

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

ListOutcomeTime frameDescription
PrimaryChange of eGFR24 monthsThe change of eGFR from baseline after 24 months of treatment
SecondaryChange of proteinuria24 monthsThe change of proteinuria from baseline after 24 months of treatment
SecondaryProgression of kidney disease24 monthsThe incidence of doubling of serum creatinine, a sustained ≥40% eGFR decline from baseline, or end-stage kidney disease after treatment
OtherChange of eGFR in different subgroups24 monthsThe change of eGFR from baseline in patients with different phenotype -genotype after treatment
OtherChange of proteinuria in different subgroups24 monthsThe change of proteinuria from baseline in patients with different phenotype -genotype after treatment

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/NCT06226896

GET https://conductscience.org/api/trials/v1/NCT06226896/registered