Trial · NCT02223949
Registered outcomes13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 13 of 13
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cesarian section rate | 24 hours | |
| Secondary | Incidence of excessive uterine activity Incidence of excessive uterine activity | 24 hours | At least 6 uterine contractions per 10- minutes period, or hyperstimulation, if combined with fetal heart rate abnormalities, or hypertonus defined as single contraction of 2-minute duration. |
| Secondary | Active labor onset | 24 hours | |
| Secondary | Proportion of vaginal delivery | 24 hours | |
| Secondary | Treatment failure | 12-24 hours | Proportion of subjects with unfavorable/unchanged Bishop score 12-24 hours after ripening |
| Secondary | The ripening-to-delivery time interval | 24 hours | |
| Secondary | Need for oxytocin induction and/or augmentation of labor | 24 hours | |
| Secondary | Mode of delivery | 24 hours | NVD vs. instrumental |
| Secondary | Intra-partum or postpartum fever | 48 hours | |
| Secondary | Incidence of meconium staining | 24 hours | |
| Secondary | The proportion of neonates with 5-minute Apgar scores of less than 7 | 48 hours | |
| Secondary | The number of neonates who were admitted to the neonatal intensive care unit | 48 hours | |
| Secondary | morbidity and mortality | 48 hours | Number of cases of serious maternal and/or neonatal morbidity or death (including uterine rupture, maternal admission to the intensive care unit, maternal septicemia, placental abruption, hemorrhage at required blood transfusion, hysterectomy, neonatal seizures, birth asphyxia, meconium aspiration syndrome, or neonatal sepsis). |
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/NCT02223949/registered