Trial · NCT04598165
Outcomes12
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Neonatal Mortality | 28 days postpartum | Intention-to-treat for participants with a known infant outcome at 6 weeks postpartum. Seventy-two (72) participants excluded from the Overall Number of Participants Analyzed, due to stillbirth. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Early Neonatal Mortality | 7 days postpartum | Intention-to-treat for participants with a known infant outcome at the 7th day of life. Seventy-two (72) stillbirths were removed from analysis cohort. This includes 13 participants for whom an outcome is not known at 6 weeks of life for the primary outcome. Seventy-two (72) stillbirths were removed from analysis cohort.Seventy-two (72) participants excluded from the Overall Number of Participants Analyzed, due to stillbirth. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Initiation of Early Breastfeeding | 1 hour postpartum | This population includes participants who did not experience a stillbirth or infant death by 2 weeks postpartum, who attended the 2 week follow-up visit, who did not decline to answer and those for whom data was not missing. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Exclusive Breastfeeding | 6-weeks postpartum | This population includes participants who did not experience a stillbirth or infant death by 6 weeks postpartum, who attended the 6 week follow-up visit, who did not decline to answer and those for whom data was not missing. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Thermal Care | 24 hours postpartum | This population includes participants who did not experience a stillbirth or infant death by 2 weeks postpartum, whose infants did not die on the first day of life, who did not decline to answer and those for whom data was not missing. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Cord Care | 2-weeks postpartum | This population includes participants who did not experience a stillbirth or infant death by 2 weeks postpartum, those who did not decline to answer and those for whom data was not missing. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Home Provision of Kangaroo Mother Care | 14 days at home postpartum | Only among preterm and/or low birth weight live births. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Maternal Knowledge of Neonatal Danger Signs | Up to 6-weeks postpartum | For this time-varying outcome, data for the 6-week visit are presented here. This population includes those who did not decline to answer and those for whom data was not missing. Data are missing for those experienced an infant loss by the 6-week visit. | Number of danger signs named | MEDIAN |
| SECONDARY | Appropriate Care-seeking | 18 weeks postpartum | Only in infants with illness episodes with danger signs and/or where the infant was hospitalized irrespective of danger signs reported. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Elevated Depressive Symptoms | Enrollment through 6-weeks postpartum | This population includes participants who attended the 6 week visit, those who did not decline to answer and those for whom data was not missing. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Social Support | Enrollment through 6-weeks postpartum | For this time-varying outcome, data for the 6-week visit are presented here. This population includes those who did not decline to answer and those for whom data was not missing. | score on a scale | MEDIAN |
| SECONDARY | Self-efficacy | Enrollment through 6-weeks postpartum | For this time-varying outcome, data for the 6-week visit are presented here. This population includes those who did not decline to answer and those for whom data was not missing. | score on a scale | MEDIAN |
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/NCT04598165/outcomes