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Trial · NCT07903922

Continuous Blood Pressure Variability and Small Vessel Disease in Acute Ischemic Stroke

NCT07903922, Recruiting, Minyoul Baik

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Continuous Blood Pressure Variability and Small Vessel Disease in Acute Ischemic Stroke. Trials, record NCT07903922. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07903922

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Trial

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

Title
Continuous Blood Pressure Variability and Small Vessel Disease in Acute Ischemic Stroke
NCT number
NCT07903922
Status
Recruiting
Enrollment
450 participants, estimated
Lead sponsor
Minyoul Baik
Conditions
Ischemic Stroke, Acute, Blood Pressure Variability, Cerebral Small Vessel Disease, White Matter Hyperintensity
Interventions
Cuffless ring-type continuous blood pressure monitor
First posted
2026-10-29
Last updated
2026-11-12

Source ClinicalTrials.gov

Registered outcomes5

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

ListOutcomeTime frameDescription
PrimaryPoor functional outcome (modified Rankin Scale 3-6) at dischargeAt discharge or transfer from the neurology service, whichever occurs first (an average of 7 days)
Functional outcome measured by the modified Rankin Scale (mRS), a 7-level scale from 0 (no symptoms) to 6 (death). Poor outcome is defined as mRS 3-6 versus good outcome mRS 0-2, assessed at hospital discharge. The primary analysis relates this outcome to systolic blood pressure variability (standard deviation) over the first 72 hours.
SecondaryOrdinal modified Rankin Scale at the end of admissionAt discharge or transfer from the neurology service, whichever occurs first (an average of 7 days)Full distribution of the modified Rankin Scale (0-6) at the end of the acute neurology admission, analyzed in relation to blood pressure variability metrics.
SecondaryEarly neurological deterioration during hospitalizationDuring the acute neurology admission (an average of 7 days)Early neurological deterioration, defined as an increase of 2 or more points in the NIHSS during the acute admission.
SecondaryParenchymal hematoma during hospitalizationDuring the acute neurology admission (an average of 7 days)Parenchymal hematoma on follow-up imaging, classified by the ECASS radiologic criteria (PH1 or PH2), during the acute neurology admission.
SecondaryPoor functional outcome (modified Rankin Scale 3-6) at 3 months90 days after stroke onset
Functional outcome is measured by the modified Rankin Scale (mRS), a 7-level scale ranging from 0 (no symptoms) to 6 (death). A poor outcome is defined as an mRS score of 3-6, compared to a good outcome of 0-2, evaluated at 3 months post-stroke if follow-up data are available.

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/NCT07903922

GET https://conductscience.org/api/trials/v1/NCT07903922/registered