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
Cite this record
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
On this page
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.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Systolic Blood Pressure | 30 days | Seated systolic blood pressure following midodrine administration compared to placebo. |
| Secondary | Cerebral Blood Flow | 30 days | Middle cerebral artery blood flow velocity following midodrine administration compared to placebo. |
| Secondary | Hopkins Verbal Learning Test | 30 days | Memory score on the Hopkins Verbal Learning Test following midodrine administration compared to placebo. Higher score is better, range from 0 to 36. |
| Secondary | Number of Hypertensive Events | 30 days | Number of daily systolic blood pressure recordings above 140 mmHg following midodrine administration compared to placebo. |
Source ClinicalTrials.gov
Outcomes4
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Systolic Blood Pressure | 30 days | mmHg | MEAN | |
| SECONDARY | Cerebral Blood Flow | 30 days | cm/sec | MEAN | |
| SECONDARY | Hopkins Verbal Learning Test | 30 days | score on a scale | MEAN | |
| SECONDARY | Number of Hypertensive Events | 30 days | blood pressure recordings | NUMBER |
Source ClinicalTrials.gov
Results by group8
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Systolic Blood Pressure | Midodrine | 116.3 | Standard Deviation 22.7 | mmHg | |
| Systolic Blood Pressure | Placebo | 98.0 | Standard Deviation 23.3 | mmHg | |
| Cerebral Blood Flow | Midodrine | 45.08 | Standard Deviation 12.87 | cm/sec | |
| Cerebral Blood Flow | Placebo | 43.97 | Standard Deviation 16.70 | cm/sec | |
| Hopkins Verbal Learning Test | Midodrine | -3.56 | Standard Deviation 4.16 | score on a scale | |
| Hopkins Verbal Learning Test | Placebo | -2.27 | Standard Deviation 6.47 | score on a scale | |
| Number of Hypertensive Events | Midodrine | 112 | blood pressure recordings | ||
| Number of Hypertensive Events | Placebo | 50 | blood pressure recordings |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Midodrine/Placebo | 8 | |
| Overall Study | STARTED | Placebo/Midodrine | 11 | |
| Overall Study | COMPLETED | Midodrine/Placebo | 3 | |
| Overall Study | COMPLETED | Placebo/Midodrine | 7 | |
| Overall Study | NOT COMPLETED | Midodrine/Placebo | 5 | |
| Overall Study | NOT COMPLETED | Placebo/Midodrine | 4 |
Source ClinicalTrials.gov
Adverse events6
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Hypertensive response | Vascular disorders | Midodrine | 3 | 19 | 3 |
| other | Hypertensive response | Vascular disorders | Placebo | 0 | 19 | 0 |
| other | UTI | Renal and urinary disorders | Midodrine | 1 | 19 | 1 |
| other | UTI | Renal and urinary disorders | Placebo | 19 | ||
| other | Constipation | Renal and urinary disorders | Midodrine | 1 | 19 | 1 |
| other | Constipation | Renal and urinary disorders | Placebo | 19 |
Source ClinicalTrials.gov
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Midodrine | 0 | 19 |
| Total, all-cause mortality | Placebo | 0 | 19 |
| Total, other adverse events | Midodrine | 5 | 19 |
| Total, other adverse events | Placebo | 0 | 19 |
| Total, serious adverse events | Midodrine | 0 | 19 |
| Total, serious adverse events | Placebo | 0 | 19 |
Source ClinicalTrials.gov
Papers2
The papers the trial lists on ClinicalTrials.gov.
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.
| Comparison | Source |
|---|---|
| Midodrine vs Placebo: deaths from any cause | Trial comparisons |
| Midodrine vs Placebo: serious adverse events | Trial comparisons |
Tests1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as |
|---|---|
| Verbal Learning | Secondary outcome |
Source ConductCognition
Data dates
The day each source was copied for this release.
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