Trial · NCT07121634
Cervical Ripening With Misoprostol vs Isosorbide Mononitrate ; A Parallel -Arm Randomized Controlled Trial
NCT07121634, Not applicable, Active not recruiting, Raid M. Al-Ani
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Cervical Ripening With Misoprostol vs Isosorbide Mononitrate ; A Parallel -Arm Randomized Controlled Trial. Trials, record NCT07121634. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07121634
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Cervical Ripening With Misoprostol vs Isosorbide Mononitrate ; A Parallel -Arm Randomized Controlled Trial
- NCT number
- NCT07121634
- Status
- Active not recruiting
- Phases
- Not applicable
- Enrollment
- 80 participants, actual
- Lead sponsor
- Raid M. Al-Ani
- Conditions
- Cervical Ripening
- Interventions
- Misoprostol 25 µg Vaginal, Isosorbide Mononitrate
- First posted
- 2025-08-13
- Last updated
- 2025-08-13
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cervical Ripening Success | Time Frame: Up to 40 hours post-intervention | Proportion of participants achieving Bishop Score ≥6 within 40 hours after receiving Misoprostol or Isosorbide Mononitrate. Unit of Measure: Percentage of participants (%) |
| Other | Cesarean Section | during delivery | Rate of Cesarean Section Proportion of participants who underwent cesarean delivery. Unit of Measure: Percentage of participants (%) |
| Other | Postpartum Hemorrhage Unit of Measure: Number of participants | Delivery to 2 hours postpartum | Number of participants with blood loss ≥500 mL during or within 2 hours after delivery. |
| Other | abnormal fetal heart tracing during labor | during delivery | number of fetuses who develop abnormal heart tracing |
| Other | Neonatal Apgar Score <7 at 1 Minute Unit of Measure: Number of neonates | Time Frame: 1 minute post-delivery | Description: Number of neonates with Apgar score \<7 at 1 minute after birth. |
| Other | Neonatal Apgar Score <10 at 5 Minutes | 5 minutes post-delivery | Number of neonates with Apgar score \<10 at 5 minutes after birth. Unit of Measure: Number of neonates |
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/NCT07121634
GET https://conductscience.org/api/trials/v1/NCT07121634/registered