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Trial · NCT07888504

Low-Dose Spironolactone in Hemodialysis Patients With Resistant Hypertension

NCT07888504, Phase 4, Completed, Universitas Sebelas Maret

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Low-Dose Spironolactone in Hemodialysis Patients With Resistant Hypertension. Trials, record NCT07888504. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07888504

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Trial

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

Title
Low-Dose Spironolactone in Hemodialysis Patients With Resistant Hypertension
NCT number
NCT07888504
Status
Completed
Phases
Phase 4
Enrollment
21 participants, actual
Lead sponsor
Universitas Sebelas Maret
Conditions
Resistant Hypertension, Kidney Failure, Chronic, Hemodialysis
Interventions
Spironolactone
First posted
2026-10-22
Last updated
2026-10-22

Source ClinicalTrials.gov

Registered outcomes10

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

ListOutcomeTime frameDescription
PrimaryChange in systolic blood pressureBaseline and week 6Office systolic blood pressure (mmHg). Change = week-6 value minus baseline value.
PrimaryChange in diastolic blood pressureBaseline and week 6Office diastolic blood pressure (mmHg). Change = week-6 value minus baseline value.
SecondaryChange in SDNNBaseline and week 6Standard deviation of normal-to-normal intervals (ms) from short-term heart rate variability recording. Change = week-6 value minus baseline value.
SecondaryChange in RMSSDBaseline and week 6Root mean square of successive differences (ms) from short-term heart rate variability recording. Change = week-6 value minus baseline value.
SecondaryChange in frequency-domain heart rate variabilityBaseline and week 6Total power, very-low-frequency power, low-frequency power, high-frequency power (ms\^2), and LF/HF ratio. Change = week-6 value minus baseline value.
SecondaryChange in serum interleukin-6Baseline and week 6Serum interleukin-6 (pg/mL) measured by ELISA. Change = week-6 value minus baseline value.
SecondaryChange in serum high-sensitivity C-reactive proteinBaseline and week 6Serum hs-CRP (mg/L) measured by particle-enhanced immunoturbidimetric assay. Change = week-6 value minus baseline value.
SecondaryChange in serum NT-proBNPBaseline and week 6Serum N-terminal pro-B-type natriuretic peptide (pg/mL) measured by ELISA. Change = week-6 value minus baseline value.
SecondaryChange in serum potassiumBaseline and week 6Serum potassium (mmol/L), the main safety measure. Change = week-6 value minus baseline value.
SecondaryChange in serum urea and creatinineBaseline and week 6Serum urea and creatinine (mg/dL). Change = week-6 value minus baseline value.

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/NCT07888504

GET https://conductscience.org/api/trials/v1/NCT07888504/registered