Name (Synonyms) | Correlation | |
---|---|---|
drug1331 | Leronlimab (700mg) Wiki | 0.71 |
drug1860 | Placebos Wiki | 0.24 |
drug1822 | Placebo Wiki | 0.06 |
Name (Synonyms) | Correlation |
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There is one clinical trial.
This study aims to test the hypothesis that a unique blend of resistant starches and fiber will promote gastrointestinal health, as measured by an increase in short-chain fatty acids and improvement in quality of life measures in conjunction with microbial community changes. This study specifically evaluates the impact on short-chain fatty acids and gut microbiota and the impact on quality of life from a resistant starch blend in healthy adult humans with occasional gastrointestinal distress.
Description: Concentration of total short-chain fatty acids, including valerate, isovalerate and isobutyrate, and individually-reported n-butyrate concentration as well as propionate and acetate % will be reported by Genova Diagnostics Report
Measure: Change in Concentration of short-chain fatty acids from baseline to each product intervention Time: Baseline (2 week period) compared to each product completion period of 2 weeksDescription: Fecal frequency (time in hours between stools) will be evaluated for each time period and compared between baseline (2 week period) and product intervention period (each 2 week period)
Measure: Change in fecal frequency (hours between stools) from baseline at each intervention Time: Baseline (2 week period) to end of product completion (2 week intervention for each dose and time combination)Description: Response pattern score on PROMIS Scale v1.0 - GI Diarrhea will be compared between baseline and each intervention period
Measure: Change in Response pattern score for Frequency and Severity of Gastrointestinal Symptoms (PROMIS Scale v1.0 - GI Diarrhea 6a) Time: Baseline (2 week period) to end of product completion (2 week intervention for each dose and time combination)Description: Response pattern score on PROMIS Scale v1.0 - GI Constipation will be compared between baseline and each intervention period
Measure: Change in Response pattern score for Frequency and Severity of Gastrointestinal Symptoms (PROMIS Scale v1.0 - GI Constipation) Time: Baseline (2 week period) to end of product completion (2 week intervention for each dose and time combination)Description: Response pattern score on PROMIS Scale v1.0 - GI Gas and Bloating 13a 09-02-2016 will be compared between baseline and each intervention period
Measure: Change in Response pattern score for Frequency and Severity of Gastrointestinal Symptoms (PROMIS Scale v1.0 - GI Gas and Bloating 13a 09-02-2016) Time: Baseline (2 week period) to end of product completion (2 week intervention for each dose and time combination)