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NCT07576881 · ClinicalTrials.gov registry record · Phase 2
Impact of Standardization on Outcomes Following Cervical Ripening
A Phase 2 study, sponsored by Indiana University.
- Not yet
- Registry status
- Phase 2
- Development phase
- 1,158
- Enrollment target
NCT07576881 is a Phase 2 study that has not yet begun recruiting, run by Indiana University. The registered enrollment target is 1,158 participants.
The verdict
NCT07576881, a Phase 2 study, has not yet begun recruiting, sponsored by Indiana University.
- NOT YET RECRUITING
- Registry status
- Phase 2
- Development phase
- 1,158 participants
- Enrollment target
Study Summary
The primary purpose of this study is to determine if vaginal delivery rate is impacted by the use of standardized methods of cervical ripening. Additional outcomes will be evaluated including maternal and fetal outcomes of labor.
Interventions
- DEVICE Cervical Ripening with a double balloon catheter only
- COMBINATION_PRODUCT Cervical ripening with a double balloon catheter plus misoprostol
- COMBINATION_PRODUCT Usual-care control group
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,158 participants |
| Start Date | 2026-06 |
| Est. Completion | 2028-04 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07576881
The ClinicalTrials.gov registry entry for NCT07576881 describes a study currently listed as not yet recruiting, categorized as Phase 2. The registered enrollment target is 1,158 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Cervical Ripening with a double balloon catheter only is the first listed.
NCT07576881 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT07576881 about?
NCT07576881 is a clinical study titled "Impact of Standardization on Outcomes Following Cervical Ripening". The primary purpose of this study is to determine if vaginal delivery rate is impacted by the use of standardized methods of cervical ripening. Additional outcomes will be evaluated including maternal and fetal outcomes of labor.
What is the current status of trial NCT07576881?
This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 1,158 participants. The study started on 2026-06. Estimated completion is 2028-04.
What interventions are being tested in trial NCT07576881?
The interventions under investigation include: Cervical Ripening with a double balloon catheter only (DEVICE), Cervical ripening with a double balloon catheter plus misoprostol (COMBINATION_PRODUCT), Usual-care control group (COMBINATION_PRODUCT).
Who is sponsoring clinical trial NCT07576881?
This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.
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