Trial · NCT05696574
Oral and Vaginal Misoprostol for Induction of Labor in Nulliparous Pregnant Women
NCT05696574, Not applicable, Unknown, Cairo University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Oral and Vaginal Misoprostol for Induction of Labor in Nulliparous Pregnant Women. Trials, record NCT05696574. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05696574
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Oral and Vaginal Misoprostol for Induction of Labor in Nulliparous Pregnant Women
- NCT number
- NCT05696574
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 80 participants, estimated
- Lead sponsor
- Cairo University
- Conditions
- Misoprostol, Labor, Nulliparous, Pregnancy
- Interventions
- Vaginal Misoprostol, Oral Misoprostol
- First posted
- 2023-01-25
- Last updated
- 2023-01-25
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Onset of active stage of labor | 24 hours postoperatively | Duration to onset of active stage of labor |
| Secondary | Cesarean section rate in each group | Within 24 hours from drug induction | Cesarean section rate will be recorded |
| Secondary | Doses given | Intraoperativley | Number of durg doses given will be recored |
| Secondary | Augmentation need | Intraoperatively | Number of participants need for labor augmentation with oxytocin and/or amniotomy will be evaluated |
| Secondary | Complications | 48 hours Postoperatively | Any complications will be recorded |
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT05696574
GET https://conductscience.org/api/trials/v1/NCT05696574/registered