Condition
Satiety in Healthy Volunteers
Total Trials
2
Recruiting
0
Active
0
Completed
2
Success Rate
100.0%+13% vs avg
Key Insights
Highlights
Success Rate
100% trial completion (above average)
Treatment Research
6 treatments under study, led by Prebiotic Soda Shelf Stable
Clinical Risk Assessment
Based on trial outcomes
Moderate Risk
Score: 50/100
Termination Rate
0.0%
0 terminated out of 2 trials
Success Rate
100.0%
+13.4% vs benchmark
Late-Stage Pipeline
0%
0 trials in Phase 3/4
Results Transparency
0%
0 of 2 completed with results
Key Signals
100% success
Data Visualizations
Phase Distribution
2Total
Not Applicable (2)
Trial Status
Completed2
Trial Success Rate
100.0%
Benchmark: 86.6%
Based on 2 completed trials
Clinical Trials (2)
Showing 2 of 2 trials
NCT07362563Not ApplicableCompletedPrimary
Effect of Prebiotic Sodas on Postprandial Levels of GLP-1, PYY, Transit Time and Satiety Levels: A Pilot Study
NCT02934321Not ApplicableCompletedPrimary
Assessment of Satiety Following Oral Administration of an Erythritol Sweetened Beverage
Showing all 2 trials
Research Network
Common Treatments
- Prebiotic Soda Shelf Stable1
- Aspartame1
- Prebiotic Soda Refrigerated1
- Erythritol1
- Prebiotic Soda Shelf Stable Functional Ingredient1
Active Sponsors
- University of Florida1
- INQUIS Clinical Research1
- Olipop, PBC1
Top Investigators
University of Florida
INQUIS Clinical Research