Trial · NCT06933056
Comparison of Antiplatelet Effects of Sotagliflozin to FDA-approved Antiplatelet Drugs
NCT06933056, Early phase 1, Completed, University of Michigan
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Antiplatelet Effects of Sotagliflozin to FDA-approved Antiplatelet Drugs. Trials, record NCT06933056. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06933056
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of Antiplatelet Effects of Sotagliflozin to FDA-approved Antiplatelet Drugs
- NCT number
- NCT06933056
- Status
- Completed
- Phases
- Early phase 1
- Enrollment
- 21 participants, actual
- Lead sponsor
- University of Michigan
- Conditions
- Platelet Function and Reactivity Tests
- Interventions
Sotagliflozin (SOTA) followed by 3 drugs in a random order, Aspirin followed by 3 drugs in a random order, Clopidogrel followed by 3 drugs in a random order, Eliquis followed by 3 drugs in a random order
- First posted
- 2025-04-18
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Platelet aggregation | Blood will be drawn and aggregation measured at baseline (day 1) and every 14 days. | Measured from blood samples |
| Secondary | Platelet granule secretion | Blood will be drawn and granule secretion measured at baseline (day 1) and every 14 days. | Measured from blood samples |
| Secondary | Total thrombus activation with T-TAS | Blood will be drawn and T-TAS measured at baseline (day 1) and every 14 days. | Measured from blood samples |
| Secondary | Thromboelastography (TEG) | Blood will be drawn and thromboelastography measured at baseline (day 1) and every 14 days. | Measured from blood samples |
| Secondary | Platelet integrin activation | Blood will be drawn and platelet integrin activation measured at baseline (day 1) and every 14 days. | Measured from blood samples |
Source ClinicalTrials.gov
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.
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/NCT06933056
GET https://conductscience.org/api/trials/v1/NCT06933056/registered