Trial · NCT04103450
Results by group24
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 24
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants With Any Serious Adverse Event, and Treatment Emergent Adverse Event (>5%) | 52-Week Vibegron Group | Any SAE | 2 | Participants | |
| Number of Participants With Any Serious Adverse Event, and Treatment Emergent Adverse Event (>5%) | 28-Week Vibegron Group | Any SAE | 3 | Participants | |
| Number of Participants With Any Serious Adverse Event, and Treatment Emergent Adverse Event (>5%) | 52-Week Vibegron Group | Any non-SAE | 17 | Participants | |
| Number of Participants With Any Serious Adverse Event, and Treatment Emergent Adverse Event (>5%) | 28-Week Vibegron Group | Any non-SAE | 3 | Participants | |
| Number of Participants With Clinically Significant Changes in Hematology Parameters | 52-Week Vibegron Group | 0 | Participants | ||
| Number of Participants With Clinically Significant Changes in Hematology Parameters | 28-Week Vibegron Group | 0 | Participants | ||
| Number of Participants With Clinically Significant Changes in Chemistry Parameters | 52-Week Vibegron Group | 0 | Participants | ||
| Number of Participants With Clinically Significant Changes in Chemistry Parameters | 28-Week Vibegron Group | 0 | Participants | ||
| Number of Participants With Clinically Significant Changes in Urinary Parameters | 52-Week Vibegron Group | 0 | Participants | ||
| Number of Participants With Clinically Significant Changes in Urinary Parameters | 28-Week Vibegron Group | 0 | Participants | ||
| Number of Participants With Clinically Significant Changes in Coagulation Parameter | 52-Week Vibegron Group | 0 | Participants | ||
| Number of Participants With Clinically Significant Changes in Coagulation Parameter | 28-Week Vibegron Group | 0 | Participants | ||
| Change From Baseline in Diastolic Blood Pressure (DBP) and Systolic Blood Pressure (SBP) | 52-Week Vibegron Group | SBP | -1.2 | Standard Deviation 12.50 | Millimeters of mercury |
| Change From Baseline in Diastolic Blood Pressure (DBP) and Systolic Blood Pressure (SBP) | 28-Week Vibegron Group | SBP | 0.1 | Standard Deviation 9.31 | Millimeters of mercury |
| Change From Baseline in Diastolic Blood Pressure (DBP) and Systolic Blood Pressure (SBP) | 52-Week Vibegron Group | DBP | 0.2 | Standard Deviation 8.79 | Millimeters of mercury |
| Change From Baseline in Diastolic Blood Pressure (DBP) and Systolic Blood Pressure (SBP) | 28-Week Vibegron Group | DBP | 1.1 | Standard Deviation 6.82 | Millimeters of mercury |
| Change From Baseline in Heart Rate | 52-Week Vibegron Group | 3.3 | Standard Deviation 9.24 | Beats per minute | |
| Change From Baseline in Heart Rate | 28-Week Vibegron Group | -0.7 | Standard Deviation 7.98 | Beats per minute | |
| Change From Baseline at Week 52 in the Average Number of Micturition Episodes Per Day | 52-Week Vibegron Group | -2.43 | Standard Error 0.299 | Micturition Episodes per Day | |
| Change From Baseline at Week 52 in the Average Number of Urgency Episodes Per Day | 52-Week Vibegron Group | -2.90 | Standard Error 0.422 | Urgency Episodes per Day |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
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 list from software.
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GET https://conductscience.org/api/trials/v1/NCT04103450/results