Trial · NCT02223949
Labor Induction and Maternal BMI, Comparison of Different Pre-induction Cervical Ripening Methods
NCT02223949, Phase 2, Phase 3, Unknown, Hillel Yaffe Medical Center
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Labor Induction and Maternal BMI, Comparison of Different Pre-induction Cervical Ripening Methods. Trials, record NCT02223949. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02223949
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Labor Induction and Maternal BMI, Comparison of Different Pre-induction Cervical Ripening Methods
- NCT number
- NCT02223949
- Status
- Unknown
- Phases
- Phase 2, Phase 3
- Enrollment
- 624 participants, estimated
- Lead sponsor
- Hillel Yaffe Medical Center
- Conditions
- Obesity, Labor Complications
- Interventions
- Cook double balloon catheter, PGE1 tablet
- First posted
- 2014-08-22
- Last updated
- 2014-08-22
Source ClinicalTrials.gov
Registered outcomes13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| 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 |
1 to 10 of 13Source ClinicalTrials.gov
See all 13 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 36996264 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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 trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT02223949
GET https://conductscience.org/api/trials/v1/NCT02223949/registered