Trial · NCT01765881
Comparison Between 25 µg Vaginal Misoprostol vs Slow Release Pessary PGE2
NCT01765881, Phase 2, Completed, University Hospital, Toulouse
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison Between 25 µg Vaginal Misoprostol vs Slow Release Pessary PGE2. Trials, record NCT01765881. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01765881
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison Between 25 µg Vaginal Misoprostol vs Slow Release Pessary PGE2
- NCT number
- NCT01765881
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 1,700 participants, actual
- Lead sponsor
- University Hospital, Toulouse
- Conditions
- Delivery Uterine
- Interventions
- Misoprostol, Dinoprostone
- First posted
- 2013-01-10
- Last updated
- 2016-04-28
- Other registries' IDs
- eudract:2011-000933-35
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cesarean for all indications | Up to delivery | Occurrence of cesarean section for all indications |
| Secondary | Cost-effectiveness of two strategies (direct medical cost differential efficiency strategies measured by the Cesarean rate | Up to discharge / end of study | |
| Other | Adverse events | Up to discharge/end of study | Summary description of all adverse events, related adverse events and serious adverse events by treatment using MedRA classification. |
| Other | Other specific safety assessments | Up to discharge/end of study | Maternal hyperstimulation syndromes with or without changes of foetal heart rate, uterine hypertonus, rate, rate of postpartum hemorrhage, degree III/IV perineal tears, uterine rupture, neonatal rate of pH \<7.05 and/or BDbase deficit\> 12mmol / L, rates Apgar score \<7 at 5 minutes, transfer rate in neonatal intensive-care unit (NICU), neonatal seizures |
| Other | Other efficacy assessments | Up to discharge/end of study | Time from 1st treatment administration to delivery, ocytocine administration and dose, occurrence of instrumental delivery, occurrence of spontaneous delivery |
| Other | Participant satisfaction assessment | Up to discharge/end of study | Maternal satisfaction using visual analog scale and questionnaire |
Source ClinicalTrials.gov
Outcomes0
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.
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 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/NCT01765881
GET https://conductscience.org/api/trials/v1/NCT01765881/registered