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NCT03171480 · ClinicalTrials.gov registry record · Phase 4
Use of Nitrous Oxide Donor for Labor Induction in Women With PreEclampsia
A Phase 4 study, sponsored by Ohio State University.
- Completed
- Registry status
- Phase 4
- Development phase
- 176
- Enrollment target
NCT03171480 is a Phase 4 study that has completed, run by Ohio State University. The registered enrollment target is 176 participants.
The verdict
NCT03171480, a Phase 4 study, has completed, sponsored by Ohio State University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 176 participants
- Enrollment target
Study Summary
A randomized controlled trial (RCT) of nitric-oxide donor (NOD) isosorbide mononitrate (IMN) versus placebo as an adjuvant to misoprostol/ intra-cervical Foley bulb for induction of labor to decrease rate of cesarean deliveries in pregnancies complicated by preeclampsia (≥24/0 weeks' gestation)
Interventions
- DRUG Placebo
- DRUG Monoket Pill
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 176 participants |
| Start Date | 2017-10-30 |
| Est. Completion | 2020-07-01 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03171480
The ClinicalTrials.gov registry entry for NCT03171480 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 176 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ohio State University, which has 552 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT03171480 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03171480 about?
NCT03171480 is a clinical study titled "Use of Nitrous Oxide Donor for Labor Induction in Women With PreEclampsia". A randomized controlled trial (RCT) of nitric-oxide donor (NOD) isosorbide mononitrate (IMN) versus placebo as an adjuvant to misoprostol/ intra-cervical Foley bulb for induction of labor to decrease rate of cesarean deliveries in pregnancies complicated by preeclampsia (≥24/0 weeks' gestation)
What is the current status of trial NCT03171480?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 176 participants. The study started on 2017-10-30. Estimated completion is 2020-07-01.
What interventions are being tested in trial NCT03171480?
The interventions under investigation include: Placebo (DRUG), Monoket Pill (DRUG).
Who is sponsoring clinical trial NCT03171480?
This trial is sponsored by Ohio State University, which has 552 total clinical trials registered on ClinicalTrials.gov.
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