Trial · NCT02408315
Outcomes11
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Time to Delivery | from study entry until delivery- anticipated 3 days | hours | MEDIAN | |
| PRIMARY | Number of Participants With Cesarean Deliveries Based on Fetal Non-Reassurance Indications | from study entry until delivery- anticipated 3 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Vaginal Deliveries That Occurred Within 24 Hours | from study entry until delivery- anticipated 3 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Participants Who Had Uterine Hyperstimulation | from study entry until delivery- anticipated 3 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Neonatal Intensive Care Unit (NICU) Admission | from study entry until discharge of newborn- anticipated up to 28 days | participants | NUMBER | |
| SECONDARY | Number of Doses Misoprostol Used | from study entry until delivery- anticipated 3 days | doses | MEDIAN | |
| SECONDARY | Uterine Rupture | from study entry until delivery- anticipated 3 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Dose of Oxytocin Used for Augmentation | from study entry until delivery- anticipated 3 days | milliunits per minute | MEDIAN | |
| SECONDARY | Number of Participants With Neonatal Cord Gases Measured | from study entry until delivery- anticipated 3 days | Participants | COUNT_OF_PARTICIPANTS | |
| OTHER_PRE_SPECIFIED | Pharmacokinetic Profiling of Misoprostol | from study entry until delivery- anticipated 3 days | |||
| OTHER_PRE_SPECIFIED | Participant Satisfaction | from study entry until discharge- anticipated 5 days |
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/NCT02408315/outcomes