Trial · NCT04492072
Misoprostol With Mechanical Dilation Versus Oxytocin With Mechanical Dilation for High-risk Pregnancy Inductions
NCT04492072, Not applicable, Completed, Thomas Jefferson University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Misoprostol With Mechanical Dilation Versus Oxytocin With Mechanical Dilation for High-risk Pregnancy Inductions. Trials, record NCT04492072. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04492072
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Misoprostol With Mechanical Dilation Versus Oxytocin With Mechanical Dilation for High-risk Pregnancy Inductions
- NCT number
- NCT04492072
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 150 participants, actual
- Lead sponsor
- Thomas Jefferson University
- Conditions
- Cesarean Section, Misoprostol, Oxytocin, High Risk Pregnancy
- Interventions
- Oxytocin, Misoprostol
- First posted
- 2020-07-30
- Last updated
- 2022-06-14
Source ClinicalTrials.gov
Registered outcomes18
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Rate of Cesarean Delivery | 48 hours | Total rate of cesarean delivery |
| Secondary | The time interval from induction-to-delivey for vaginal deliveries | 48 hours | Maternal outcome |
| Secondary | The number of vaginal births within 24 hours | 24 hours | Maternal outcome |
| Secondary | The number of misoprostol doses received by each participant | 24 hours | Maternal outcome |
| Secondary | The incidence of uterine tachysystole | 24 hours | Defined as greater than 5 contractions in a ten minute window, averaged over 30 minutes |
| Secondary | The rate of each indication for the cesarean delivery | 48 hours | Indications include non-reassuring fetal hear tones, arrest of dilation, arrest in the 2nd stage of labor etc. |
| Secondary | The rate of operative vaginal delivery | 48 hours | Maternal outcome - includes forceps or vacuum assisted deliveries |
| Secondary | The rate of intra-amniotic infection | 48 hours | Maternal outcome |
| Secondary | The rate of postpartum hemorrhage | 24 hours | Maternal outcome |
| Secondary | The rate of Fetal heart rate abnormaliies | 48 hours | recurrent late decelerations, bradycardia, or prolonged deceleration |
1 to 10 of 18Source ClinicalTrials.gov
See all 18 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 |
|---|---|
| 37806650 | 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/NCT04492072
GET https://conductscience.org/api/trials/v1/NCT04492072/registered