Trial · NCT04733157
Outcomes17
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 17 of 17
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Postpartum Hemorrhage (PPH) | Up to day 2 postpartum | Postpartum hemorrhage defined as having a blood loss greater than or equal to 1000 mL using change in hemoglobin values. In the clinical trial, some participants in both arms had missing data because they did not have their laboratory measurements for hemoglobin done. In Group A (93 participants) and in Group B (87 participants) had missing assessments for PPH. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Blood Loss Using Hemoglobin Values | Up to day 2 postpartum | Average blood loss in mL calculated using laboratory hemoglobin values collected from participants before and after procedure. | mL | MEAN |
| SECONDARY | Mean Blood Loss as Estimated by Obstetrician | 2 hours | Missing data for some participants due to estimates not being done at the time of delivery. | mL | MEAN |
| SECONDARY | Occurrence of Postpartum Shock | Up to day 2 postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Use of Supplementary Uterotonic(s) | Up to day 2 postpartum | Missing information about additional uterotonics for some participants due to data entry issues after delivery. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Postpartum Transfusion | Up to day 2 postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Emergency Surgery for PPH | Up to day 2 postpartum | Missing information from some participants due to data entry issues. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Change in Peripartum Haemoglobin | Up to day 2 postpartum | Missing values due to missing information if blood draws were not done within the required time frame. | g/dL | MEAN |
| SECONDARY | Number of Participants With a Decrease in Peripartum Hemoglobin | Up to day 2 postpartum | Missing data a result of laboratory specimens not being collected at the expected time from participants | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Change in Peripartum Haematocrit | Up to day 2 postpartum | Missing data due laboratory measurements not being done for some participants as samples were not taken within required time frame. | percent of hematocrit change | MEAN |
| SECONDARY | Admission Into Intensive Care Unit | Up to day 2 postpartum | data entry error for missing participant data | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Death From Any Cause | Up to date of death or day 4 from admission | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Blood Pressure Measurements | Up to 2 hours after the caesarean section | Some participants did not have their systolic and diastolic blood pressure measurements done (missing data) | mmHg | MEAN |
| SECONDARY | Number of Mild Adverse Events | Up to 24 hours after administration | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Severe Adverse Events | Up to day 3 postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Any Other Unexpected Adverse Event | Up to day 3 postpartum | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Length of Hospital Stay | Up to day 3 postpartum | Missing data due to data entry errors | days | MEAN |
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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT04733157/outcomes