Trial · NCT00948298
Effect of Vitamin D3 on Vascular Function
NCT00948298, Not applicable, Completed, Charles Drew University of Medicine and Science; results first posted 2018-07-17
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Vitamin D3 on Vascular Function. Trials, record NCT00948298. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00948298
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Vitamin D3 on Vascular Function
- NCT number
- NCT00948298
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 130 participants, actual
- Lead sponsor
- Charles Drew University of Medicine and Science
- Conditions
- Vitamin D Deficiency
- Interventions
- Vitamin D, Placebo
- First posted
- 2009-07-29
- Last updated
- 2018-07-17
- Results first posted
- 2018-07-17
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Pulse Wave Velocity for Vascular Stiffness | 12 Weeks | The primary outcome variable is pulse wave velocity (PWV) for vascular stiffness. The hypothesis is that a greater decrease in the PWV will occur with the Vitamin D3 treatment. PWV is the speed at which the arterial pulse wave travels through the arteries in the cardiovascular system. It is considered the gold standard for the assessment of arterial elastance (stiffness) and determined by radial artery applanation tonometry using the SphygmoCor device. |
| Secondary | Changes in Sitting and 24 Ambulatory Blood Pressure | 12 weeks | Improved vascular function as determined by measuring sitting and 24 Hour Ambulatory Blood Pressure. |
Source ClinicalTrials.gov
Outcomes2
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Pulse Wave Velocity for Vascular Stiffness | 12 Weeks | m/s | MEAN | |
| SECONDARY | Changes in Sitting and 24 Ambulatory Blood Pressure | 12 weeks | mmHg | MEAN |
Source ClinicalTrials.gov
Results by group10
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Pulse Wave Velocity for Vascular Stiffness | Placebo | 29.3 | Standard Deviation 11.0 | m/s | |
| Pulse Wave Velocity for Vascular Stiffness | Vitamin D | 27.6 | Standard Deviation 11.0 | m/s | |
| Changes in Sitting and 24 Ambulatory Blood Pressure | Placebo | Blood Pressure (Systolic) | 125.8 | Standard Deviation 13.3 | mmHg |
| Changes in Sitting and 24 Ambulatory Blood Pressure | Vitamin D | Blood Pressure (Systolic) | 126.9 | Standard Deviation 15.0 | mmHg |
| Changes in Sitting and 24 Ambulatory Blood Pressure | Placebo | Blood Pressure (Diastolic) | 82.2 | Standard Deviation 9.2 | mmHg |
| Changes in Sitting and 24 Ambulatory Blood Pressure | Vitamin D | Blood Pressure (Diastolic) | 81.1 | Standard Deviation 12.0 | mmHg |
| Changes in Sitting and 24 Ambulatory Blood Pressure | Placebo | 24 Hour Blood Pressure (Systolic) | 128.4 | Standard Deviation 14.0 | mmHg |
| Changes in Sitting and 24 Ambulatory Blood Pressure | Vitamin D | 24 Hour Blood Pressure (Systolic) | 127.4 | Standard Deviation 16.4 | mmHg |
| Changes in Sitting and 24 Ambulatory Blood Pressure | Placebo | 24 Hour Blood Pressure (Diastolic) | 83.9 | Standard Deviation 10.1 | mmHg |
| Changes in Sitting and 24 Ambulatory Blood Pressure | Vitamin D | 24 Hour Blood Pressure (Diastolic) | 82.0 | Standard Deviation 11.6 | mmHg |
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 | Placebo | 65 | |
| Overall Study | STARTED | Vitamin D | 65 | |
| Overall Study | COMPLETED | Placebo | 55 | |
| Overall Study | COMPLETED | Vitamin D | 60 | |
| Overall Study | NOT COMPLETED | Placebo | 10 | |
| Overall Study | NOT COMPLETED | Vitamin D | 5 |
Source ClinicalTrials.gov
Adverse events64
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 | Hemoglobin = 9.6 G/DL | Blood and lymphatic system disorders | Placebo | 0 | 65 | 0 |
| other | Hemoglobin = 9.6 G/DL | Blood and lymphatic system disorders | Vitamin D | 1 | 65 | 1 |
| other | High Platelet Count = 493 Thousand/UL | Blood and lymphatic system disorders | Placebo | 1 | 65 | 1 |
| other | High Platelet Count = 493 Thousand/UL | Blood and lymphatic system disorders | Vitamin D | 0 | 65 | 0 |
| other | Hematocrit = 30.2% | Blood and lymphatic system disorders | Placebo | 0 | 65 | 0 |
| other | Hematocrit = 30.2% | Blood and lymphatic system disorders | Vitamin D | 1 | 65 | 1 |
| other | Elevated WBC = 14.9 | Blood and lymphatic system disorders | Placebo | 0 | 65 | 0 |
| other | Elevated WBC = 14.9 | Blood and lymphatic system disorders | Vitamin D | 1 | 65 | 1 |
| other | Low White Blood Cell Count = 2.9 | Blood and lymphatic system disorders | Placebo | 0 | 65 | 0 |
| other | Low White Blood Cell Count = 2.9 | Blood and lymphatic system disorders | Vitamin D | 1 | 65 | 1 |
1 to 10 of 64Source ClinicalTrials.gov
See all 64 adverse eventsAdverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Placebo | 0 | 65 |
| Total, all-cause mortality | Vitamin D | 0 | 65 |
| Total, other adverse events | Placebo | 12 | 65 |
| Total, other adverse events | Vitamin D | 14 | 65 |
| Total, serious adverse events | Placebo | 4 | 65 |
| Total, serious adverse events | Vitamin D | 4 | 65 |
Source ClinicalTrials.gov
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants1
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.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years |
|---|---|---|---|---|---|
| U54RR022762 | Drew RCMI Translational Research Network | NORRIS, KEITH C | CHARLES R. DREW UNIVERSITY OF MED & SCI | NATIONAL CENTER FOR RESEARCH RESOURCES | 2007 to 2011 |
Source NIH RePORTER
Trial comparisons2
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Vitamin D vs Placebo: deaths from any cause | Trial comparisons |
| Vitamin D vs Placebo: serious adverse events | Trial 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.
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/NCT00948298
GET https://conductscience.org/api/trials/v1/NCT00948298/events?page=2