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Trial · NCT03482440

Angiotensin II and Chronic Inflammation in Persistent Microvascular Dysfunction Following Preeclampsia

NCT03482440, Early phase 1, Completed, University of Iowa; results first posted 2025-06-03

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Angiotensin II and Chronic Inflammation in Persistent Microvascular Dysfunction Following Preeclampsia. Trials, record NCT03482440. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03482440

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Trial

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

Title
Angiotensin II and Chronic Inflammation in Persistent Microvascular Dysfunction Following Preeclampsia
NCT number
NCT03482440
Status
Completed
Phases
Early phase 1
Enrollment
24 participants, actual
Lead sponsor
University of Iowa
Conditions
Preeclampsia
Interventions
Salsalate Oral Tablet, Placebo Oral Tablet
First posted
2018-03-29
Last updated
2025-06-03
Results first posted
2025-06-03

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryMicrovascular Endothelial Function (Cutaneous Conductance, %Maximum)immediately following the 4 days or oral treatment (salsalate or placebo)
Endothelium-dependent vasodilation assessed as cutaneous conductance response (cutaneous conductance = local red blood cell flux/mean arterial pressure; %maximum) to exogenous acetylcholine delivered via intradermal microdialysis.
SecondaryPeripheral Blood Mononuclear Cell Inflammatory Response to Ang IIat the completion of 4 days of oral (placebo or salsalate) treatmentinflammatory cytokine (TNFalpha) release by peripheral blood mononuclear cells isolated from fresh whole blood collected via venipuncture and stimulated with angiotensin II ex vivo.

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMicrovascular Endothelial Function (Cutaneous Conductance, %Maximum)immediately following the 4 days or oral treatment (salsalate or placebo)% of maximal cutaneous conductanceMEAN
SECONDARYPeripheral Blood Mononuclear Cell Inflammatory Response to Ang IIat the completion of 4 days of oral (placebo or salsalate) treatmentng/mlMEAN

Results by group4

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

OutcomeGroupCategoryValueSpreadUnits
Microvascular Endothelial Function (Cutaneous Conductance, %Maximum)Oral Salsalate95Standard Deviation 6% of maximal cutaneous conductance
Microvascular Endothelial Function (Cutaneous Conductance, %Maximum)Oral Placebo77Standard Deviation 8% of maximal cutaneous conductance
Peripheral Blood Mononuclear Cell Inflammatory Response to Ang IIOral Salsalate2.37Standard Deviation 1.28ng/ml
Peripheral Blood Mononuclear Cell Inflammatory Response to Ang IIOral Placebo2.77Standard Deviation 1.01ng/ml

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPlacebo Then Salsalate13
Overall StudySTARTEDSalsalate Then Placebo10
Overall StudyCOMPLETEDPlacebo Then Salsalate13
Overall StudyCOMPLETEDSalsalate Then Placebo10
Overall StudyNOT COMPLETEDPlacebo Then Salsalate0
Overall StudyNOT COMPLETEDSalsalate Then Placebo0

Adverse events2

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

TypeEventOrgan systemGroupAffectedAt riskEvents
othertennitis while on salsalateEar and labyrinth disordersPlacebo0230
othertennitis while on salsalateEar and labyrinth disordersSalsalate2232

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPlacebo023
Total, all-cause mortalitySalsalate023
Total, other adverse eventsPlacebo023
Total, other adverse eventsSalsalate223
Total, serious adverse eventsPlacebo023
Total, serious adverse eventsSalsalate023

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 comparisons2

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

ComparisonSource
Salsalate vs Placebo: deaths from any causeTrial comparisons
Salsalate vs Placebo: serious adverse eventsTrial comparisons

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/NCT03482440

GET https://conductscience.org/api/trials/v1/NCT03482440/registered