Trial · NCT00576420
Results by group237
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 237
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | FS VH S/D 500 S-apr- 60-Seconds | Primary Hemostasis Achieved at 4 Minutes | 46.2 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | FS VH S/D 500 S-apr - 120-Seconds | Primary Hemostasis Achieved at 4 Minutes | 62.5 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | Control Group | Primary Hemostasis Achieved at 4 Minutes | 34.8 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | FS VH S/D 500 S-apr- 60-Seconds | Additional Treatment Required for Hemostasis | 30.8 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | FS VH S/D 500 S-apr - 120-Seconds | Additional Treatment Required for Hemostasis | 25.0 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | Control Group | Additional Treatment Required for Hemostasis | 52.2 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | FS VH S/D 500 S-apr- 60-Seconds | Intraoperative Rebleeding After Primary Hemostasis | 3.8 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | FS VH S/D 500 S-apr - 120-Seconds | Intraoperative Rebleeding After Primary Hemostasis | 0.0 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Study Suture Line. | Control Group | Intraoperative Rebleeding After Primary Hemostasis | 4.3 | percentage of participants | |
| 90% Confidence Interval for the Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Suture Line | FS VH S/D 500 S-apr - 60-Seconds | 46.2 | 90% Confidence Interval 30.1 to 62.2 | percentage of participants | |
| 90% Confidence Interval for the Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Suture Line | FS VH S/D 500 S-apr - 120-Seconds | 62.5 | 90% Confidence Interval 46.2 to 78.8 | percentage of participants | |
| 90% Confidence Interval for the Percentage of Participants Achieving Hemostasis at 4 Minutes After Treatment Application at the Suture Line | Control Group | 34.8 | 90% Confidence Interval 18.4 to 51.1 | percentage of participants | |
| Hemostasis at 4 Minutes After Treatment Application at the Suture Line by Bleeding Severity - Moderate Bleeding | FS VH S/D 500 S-apr - 60-Seconds | 50.0 | 90% Confidence Interval 28.0 to 72.0 | percentage of participants | |
| Hemostasis at 4 Minutes After Treatment Application at the Suture Line by Bleeding Severity - Moderate Bleeding | FS VH S/D 500 S-apr - 120-Seconds | 66.7 | 90% Confidence Interval 44.3 to 89.1 | percentage of participants | |
| Hemostasis at 4 Minutes After Treatment Application at the Suture Line by Bleeding Severity - Moderate Bleeding | Control Group | 38.5 | 90% Confidence Interval 16.3 to 60.7 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 6 Minutes | FS VH S/D 500 S-apr - 60-Seconds | 61.5 | 90% Confidence Interval 45.8 to 77.2 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 6 Minutes | FS VH S/D 500 S-apr - 120-Seconds | 75.0 | 90% Confidence Interval 60.5 to 89.5 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 6 Minutes | Control Group | 34.8 | 90% Confidence Interval 18.4 to 51.1 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 10 Minutes | FS VH S/D 500 S-apr - 60-Seconds | 65.4 | 90% Confidence Interval 50.0 to 80.7 | percentage of participants | |
| Percentage of Participants Achieving Hemostasis at 10 Minutes | FS VH S/D 500 S-apr - 120-Seconds | 75.0 | 90% Confidence Interval 60.5 to 89.5 | percentage of participants |
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/NCT00576420/results