Trial · NCT03824938
Aspirin for Exercise in Multiple Sclerosis (ASPIRE)
NCT03824938, Phase 3, Completed, Columbia University; results first posted 2023-10-27
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Aspirin for Exercise in Multiple Sclerosis (ASPIRE). Trials, record NCT03824938. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03824938
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Aspirin for Exercise in Multiple Sclerosis (ASPIRE)
- NCT number
- NCT03824938
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 60 participants, actual
- Lead sponsor
- Columbia University
- Conditions
- Multiple Sclerosis
- Interventions
- Aspirin 650mg Oral Capsule, Acetaminophen Tablet 650mg, Placebo
- First posted
- 2019-01-31
- Last updated
- 2023-10-27
- Results first posted
- 2023-10-27
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time-to-exhaustion | from start of exercise test until self-reported exhaustion, up to 30 minutes | Duration of time exercising before reaching peak exertion, defined as cadence drop below 40 revolutions per minute (RPM) for \>/= 5 seconds, or patient reaches volitional exhaustion in accordance with American Thoracic Society standard test termination criteria. |
| Primary | Exercise-induced Body Temperature Change | from start of exercise test until self-reported exhaustion, up to 30 minutes | Change in body temperature from pre- to post- maximal exercise test. |
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 | Time-to-exhaustion | from start of exercise test until self-reported exhaustion, up to 30 minutes | seconds | MEAN | |
| PRIMARY | Exercise-induced Body Temperature Change | from start of exercise test until self-reported exhaustion, up to 30 minutes | degrees Fahrenheit | MEAN |
Source ClinicalTrials.gov
Results by group6
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Time-to-exhaustion | Placebo | 551.7 | Standard Deviation 78.4 | seconds | |
| Time-to-exhaustion | Aspirin | 331.6 | Standard Deviation 76.6 | seconds | |
| Time-to-exhaustion | Acetaminophen | 578.2 | Standard Deviation 82.1 | seconds | |
| Exercise-induced Body Temperature Change | Placebo | 0.68 | Standard Deviation 0.35 | degrees Fahrenheit | |
| Exercise-induced Body Temperature Change | Aspirin | 0.006 | Standard Deviation 0.32 | degrees Fahrenheit | |
| Exercise-induced Body Temperature Change | Acetaminophen | 0.31 | Standard Deviation 0.35 | degrees Fahrenheit |
Source ClinicalTrials.gov
Participant flow18
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Placebo First, Then Aspirin, Then Acetaminophen | 7 | |
| Overall Study | STARTED | Placebo First, Then Acetaminophen, Then Aspirin | 8 | |
| Overall Study | STARTED | Aspirin First, Then Placebo, Then Acetaminophen | 7 | |
| Overall Study | STARTED | Aspirin First, Then Acetaminophen, Then Placebo | 5 | |
| Overall Study | STARTED | Acetaminophen First, Then Placebo, Then Aspirin | 7 | |
| Overall Study | STARTED | Acetaminophen First, Then Aspirin, Then Placebo | 3 | |
| Overall Study | COMPLETED | Placebo First, Then Aspirin, Then Acetaminophen | 5 | |
| Overall Study | COMPLETED | Placebo First, Then Acetaminophen, Then Aspirin | 6 | |
| Overall Study | COMPLETED | Aspirin First, Then Placebo, Then Acetaminophen | 7 | |
| Overall Study | COMPLETED | Aspirin First, Then Acetaminophen, Then Placebo | 3 |
1 to 10 of 18Source ClinicalTrials.gov
See all 18 participant flowAdverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals9
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Placebo | 0 | 32 |
| Total, all-cause mortality | Aspirin | 0 | 31 |
| Total, all-cause mortality | Acetaminophen | 0 | 32 |
| Total, other adverse events | Placebo | 0 | 32 |
| Total, other adverse events | Aspirin | 0 | 31 |
| Total, other adverse events | Acetaminophen | 0 | 32 |
| Total, serious adverse events | Placebo | 0 | 32 |
| Total, serious adverse events | Aspirin | 0 | 31 |
| Total, serious adverse events | Acetaminophen | 0 | 32 |
Source ClinicalTrials.gov
Papers2
The papers the trial lists on ClinicalTrials.gov.
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 |
|---|---|---|---|---|---|
| R21HD091836 | Aspirin before Exercise: Antipyretic pretreatment to reduce exercise-induced overheating and exhaustion in RRMS patients | LEAVITT, VICTORIA M | COLUMBIA UNIVERSITY HEALTH SCIENCES | EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT | 2019 to 2020 |
Source NIH RePORTER
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.
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/NCT03824938
GET https://conductscience.org/api/trials/v1/NCT03824938/registered