Trial · NCT07882264
Fiber Soda on Postprandial Risk Factors
NCT07882264, Not applicable, Recruiting, Ball State University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Fiber Soda on Postprandial Risk Factors. Trials, record NCT07882264. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07882264
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Fiber Soda on Postprandial Risk Factors
- NCT number
- NCT07882264
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 20 participants, estimated
- Lead sponsor
- Ball State University
- Conditions
- Healthy Participants
- Interventions
- Prebiotic soda followed by high-fat meal, Control beverage followed by high-fat meal
- First posted
- 2026-10-20
- Last updated
- 2026-10-20
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Triglycerides | Through the study completion, up to 1 year | The investigators will measure triglycerides at baseline and 30-, 60-, 120-, 180-and 240-minutes after each meal. These measurements will take place immediately and a complete dataset will be compiled upon study completion. |
| Primary | sCD14 | Through study completion, up to 1 year. | The investigators will measure soluble CD14 at baseline and 30-, 60-, 120-, 180-and 240-minutes after each meal. These measurements will take place immediately and a complete dataset will be compiled upon study completion. |
| Primary | LBP | Through the study completion, up to 1 year | The investigators will measure LBP at baseline and 30-, 60-, 120-, 180-, 240-minutes after each meal. These measurements will take place immediately and a complete dataset will be compiled upon study completion. |
| Primary | HDL-C | Through the study completion, up to 1 year | The investigators will measure HDL-C at baseline and 30-, 60-, 120-, 180-and 240-minutes after each meal. These measurements will take place immediately and a complete dataset will be compiled upon study completion. |
| Primary | Glucose | Through the study completion, up to 1 year | The investigators will measure glucose at baseline and 30-, 60-, 120-, 180-and 240-minutes after each meal. These measurements will take place immediately and a complete dataset will be compiled upon study completion. |
| Primary | ApoB | Through the study completion, up to 1 year | The investigators will measure ApoB at baseline and 30-, 60-, 120-, 180-and 240-minutes after each meal. These measurements will take place immediately and a complete dataset will be compiled upon study completion. |
| Primary | Insulin | Through the study completion, up to 1 year | The investigators will measure insulin at baseline and 30-, 60-, 120-, 180-and 240-minutes after each meal. These measurements will take place immediately and a complete dataset will be compiled upon study completion. |
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/NCT07882264
GET https://conductscience.org/api/trials/v1/NCT07882264/registered