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NCT06498908 · ClinicalTrials.gov registry record · Phase 3
Intracervical Balloon Placement With Nitrous Oxide Administration
A Phase 3 study of Labor Pain and Induced; Birth, sponsored by Maimonides Medical Center.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 162
- Enrollment target
- 1
- Study location
NCT06498908 is a Phase 3 study of Labor Pain and Induced; Birth that is actively recruiting participants, run by Maimonides Medical Center. The registered enrollment target is 162 participants, below the 192-participant average among 14 other Labor Pain trials with a reported enrollment target (16% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06498908, a Phase 3 study of Labor Pain and Induced; Birth, is actively recruiting participants, sponsored by Maimonides Medical Center.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 162 participants
- Enrollment target
- 1
- Study location
Study Summary
This randomized controlled trial aims to compare the effectiveness of nitrous oxide versus oxygen in facilitating the successful placement of a Foley balloon catheter for cervical ripening and induction of labor.
Conditions Studied
Interventions
- DRUG Nitrous oxide
- DRUG Oxygen
Study Locations (1)
New York
- Maimonides Medical Center OB/GYN - Brooklyn
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 162 participants |
| Start Date | 2024-05-15 |
| Est. Completion | 2025-09-01 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06498908
The ClinicalTrials.gov registry entry for NCT06498908 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 162 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 192-participant average among 14 other Labor Pain trials with a reported enrollment target (16% lower). The listed sponsor is Maimonides Medical Center, which has 39 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Labor Pain appearing as the primary indexed condition, and to 2 interventions - of which Nitrous oxide is the first listed.
NCT06498908 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT06498908 about?
NCT06498908 is a clinical study titled "Intracervical Balloon Placement With Nitrous Oxide Administration". This randomized controlled trial aims to compare the effectiveness of nitrous oxide versus oxygen in facilitating the successful placement of a Foley balloon catheter for cervical ripening and induction of labor.
What is the current status of trial NCT06498908?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 162 participants. The study started on 2024-05-15. Estimated completion is 2025-09-01.
What conditions does trial NCT06498908 study?
This clinical trial studies the following conditions: Labor Pain, Induced; Birth.
What interventions are being tested in trial NCT06498908?
The interventions under investigation include: Nitrous oxide (DRUG), Oxygen (DRUG).
Who is sponsoring clinical trial NCT06498908?
This trial is sponsored by Maimonides Medical Center, which has 39 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06498908 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.