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Trial · NCT02307565

Blood Pressure, Cerebral Blood Flow and Cognition in Spinal Cord Injury

NCT02307565, Phase 3, Completed, James J. Peters Veterans Affairs Medical Center; results first posted 2025-02-21

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Blood Pressure, Cerebral Blood Flow and Cognition in Spinal Cord Injury. Trials, record NCT02307565. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02307565

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Trial

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

Title
Blood Pressure, Cerebral Blood Flow and Cognition in Spinal Cord Injury
NCT number
NCT02307565
Status
Completed
Phases
Phase 3
Enrollment
19 participants, actual
Lead sponsor
James J. Peters Veterans Affairs Medical Center
Conditions
Spinal Cord Injury
Interventions
Midodrine, Placebo
First posted
2014-12-04
Last updated
2025-02-21
Results first posted
2025-02-21

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimarySystolic Blood Pressure30 daysSeated systolic blood pressure following midodrine administration compared to placebo.
SecondaryCerebral Blood Flow30 daysMiddle cerebral artery blood flow velocity following midodrine administration compared to placebo.
SecondaryHopkins Verbal Learning Test30 daysMemory score on the Hopkins Verbal Learning Test following midodrine administration compared to placebo. Higher score is better, range from 0 to 36.
SecondaryNumber of Hypertensive Events30 daysNumber of daily systolic blood pressure recordings above 140 mmHg following midodrine administration compared to placebo.

Outcomes4

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYSystolic Blood Pressure30 daysmmHgMEAN
SECONDARYCerebral Blood Flow30 dayscm/secMEAN
SECONDARYHopkins Verbal Learning Test30 daysscore on a scaleMEAN
SECONDARYNumber of Hypertensive Events30 daysblood pressure recordingsNUMBER

Results by group8

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

OutcomeGroupCategoryValueSpreadUnits
Systolic Blood PressureMidodrine116.3Standard Deviation 22.7mmHg
Systolic Blood PressurePlacebo98.0Standard Deviation 23.3mmHg
Cerebral Blood FlowMidodrine45.08Standard Deviation 12.87cm/sec
Cerebral Blood FlowPlacebo43.97Standard Deviation 16.70cm/sec
Hopkins Verbal Learning TestMidodrine-3.56Standard Deviation 4.16score on a scale
Hopkins Verbal Learning TestPlacebo-2.27Standard Deviation 6.47score on a scale
Number of Hypertensive EventsMidodrine112blood pressure recordings
Number of Hypertensive EventsPlacebo50blood pressure recordings

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMidodrine/Placebo8
Overall StudySTARTEDPlacebo/Midodrine11
Overall StudyCOMPLETEDMidodrine/Placebo3
Overall StudyCOMPLETEDPlacebo/Midodrine7
Overall StudyNOT COMPLETEDMidodrine/Placebo5
Overall StudyNOT COMPLETEDPlacebo/Midodrine4

Adverse events6

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherHypertensive responseVascular disordersMidodrine3193
otherHypertensive responseVascular disordersPlacebo0190
otherUTIRenal and urinary disordersMidodrine1191
otherUTIRenal and urinary disordersPlacebo19
otherConstipationRenal and urinary disordersMidodrine1191
otherConstipationRenal and urinary disordersPlacebo19

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMidodrine019
Total, all-cause mortalityPlacebo019
Total, other adverse eventsMidodrine519
Total, other adverse eventsPlacebo019
Total, serious adverse eventsMidodrine019
Total, serious adverse eventsPlacebo019

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
32203065DERIVEDPubMed
33177997DERIVEDPubMed

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
Midodrine vs Placebo: deaths from any causeTrial comparisons
Midodrine vs Placebo: serious adverse eventsTrial comparisons

Tests1

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

TestNamed as
Verbal LearningSecondary outcome

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/NCT02307565

GET https://conductscience.org/api/trials/v1/NCT02307565/registered