Trial · NCT01402050
Foley Catheter Versus Cervidil for Induction of Labor at Term
NCT01402050, Not applicable, Completed, Pediatrix; results first posted 2020-02-06
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Foley Catheter Versus Cervidil for Induction of Labor at Term. Trials, record NCT01402050. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01402050
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Foley Catheter Versus Cervidil for Induction of Labor at Term
- NCT number
- NCT01402050
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 376 participants, actual
- Lead sponsor
- Pediatrix
- Conditions
- Labor Induction
- Interventions
- CERVIDIL (Dinoprostone), FOLEY BALLOON
- First posted
- 2011-07-26
- Last updated
- 2020-03-02
- Results first posted
- 2020-02-06
Source ClinicalTrials.gov
Registered outcomes1
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time Of Start Of Induction Of Labor To Delivery | Hours | The primary outcome variable was time (measured in hours) from first attempt at study agent placement to delivery. Time of placement of Labor Induction agent was noted as the time of Labor Induction initiation and time of delivery was noted as the end time of Labor Induction. There were no specific time points at which the outcomes were measured due to the uncertainty of the labor process. Total time duration of Labor induction was noted in hours. Key word: INDUCTION OF LABOR |
Source ClinicalTrials.gov
Outcomes1
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Time Of Start Of Induction Of Labor To Delivery | Hours | hours | MEDIAN |
Source ClinicalTrials.gov
Results by group2
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Time Of Start Of Induction Of Labor To Delivery | FOLEY BALLOON | 21.6 | Inter-Quartile Range 15.7 to 35.1 | hours | |
| Time Of Start Of Induction Of Labor To Delivery | CERVIDIL | 26.6 | Inter-Quartile Range 19.0 to 37.8 | hours |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | FOLEY BALLOON | 185 | |
| Overall Study | STARTED | CERVIDIL | 191 | |
| Overall Study | COMPLETED | FOLEY BALLOON | 185 | |
| Overall Study | COMPLETED | CERVIDIL | 191 | |
| Overall Study | NOT COMPLETED | FOLEY BALLOON | 0 | |
| Overall Study | NOT COMPLETED | CERVIDIL | 0 |
Source ClinicalTrials.gov
Adverse events2
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Neonatal event | Gastrointestinal disorders | FOLEY BALLOON | 0 | 185 | 0 |
| other | Neonatal event | Gastrointestinal disorders | CERVIDIL | 2 | 191 | 2 |
Source ClinicalTrials.gov
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | FOLEY BALLOON | ||
| Total, all-cause mortality | CERVIDIL | ||
| Total, other adverse events | FOLEY BALLOON | 0 | 185 |
| Total, other adverse events | CERVIDIL | 2 | 191 |
| Total, serious adverse events | FOLEY BALLOON | 0 | 185 |
| Total, serious adverse events | CERVIDIL | 0 | 191 |
Source ClinicalTrials.gov
Papers2
The papers the trial lists on ClinicalTrials.gov.
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 comparisons1
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison |
|---|
| FOLEY BALLOON vs CERVIDIL: serious adverse events |
Source Trial comparisons
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/NCT01402050
GET https://conductscience.org/api/trials/v1/NCT01402050/registered