Trial · NCT03136445
Results by group78
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 78
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
The Proportion of Patients Who Die or Have Bleeding of WHO Grade 2 or Above by WHO Criteria During the First 30 Days From the First Dose of Trial Treatment, or Planned First Dose for Those Participants Who do Not Receive Treatment. | Intervention Arm | 31.7 | 95% Confidence Interval 26.6 to 37.4 | percentage of participants | |
The Proportion of Patients Who Die or Have Bleeding of WHO Grade 2 or Above by WHO Criteria During the First 30 Days From the First Dose of Trial Treatment, or Planned First Dose for Those Participants Who do Not Receive Treatment. | Control Arm | 34.2 | 95% Confidence Interval 29.0 to 40.0 | percentage of participants | |
| Mean (SD) Percentage of Days With WHO Grade 2 Bleeding or Above, Per Participant. | Intervention Arm | 3.1 | Standard Deviation 9.5 | percentage of days | |
| Mean (SD) Percentage of Days With WHO Grade 2 Bleeding or Above, Per Participant. | Control Arm | 3.2 | Standard Deviation 7.8 | percentage of days | |
| Time to First Episode of Bleeding of WHO Grade 2 or Greater up to Study Day 30. | Intervention Arm | NA | Inter-Quartile Range 10.5 to NA | Lower quartile for number of days | |
| Time to First Episode of Bleeding of WHO Grade 2 or Greater up to Study Day 30. | Control Arm | NA | Inter-Quartile Range 8.5 to NA | Lower quartile for number of days | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Intervention Arm | Grade 0 | 7 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Control Arm | Grade 0 | 6 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Intervention Arm | Grade unassigned | 0 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Control Arm | Grade unassigned | 1 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Intervention Arm | Grade 2 | 85 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Control Arm | Grade 2 | 93 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Intervention Arm | Grade 3 | 0 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Control Arm | Grade 3 | 3 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Intervention Arm | Grade 4 | 2 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Control Arm | Grade 4 | 1 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Intervention Arm | Grade 1 | 111 | Participants | |
| Highest Grade of Bleeding a Patient Experiences up to Study Day 30. | Control Arm | Grade 1 | 121 | Participants | |
| Number of Platelet Transfusions Per Patient up to Study Day 30. | Intervention Arm | 3 | Inter-Quartile Range 1 to 6 | platelet units | |
| Number of Platelet Transfusions Per Patient up to Study Day 30. | Control Arm | 3 | Inter-Quartile Range 1 to 6 | platelet units |
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.
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GET https://conductscience.org/api/trials/v1/NCT03136445/results