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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: Recruiting Phase 3 study of Labor Pain and Induced; Birth, sponsored by Maimonides Medical Center.
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. According to ClinicalTrials.gov, the official US trial registry.
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 |
What NCT06498908 shows while recruiting
NCT06498908 is an interventional study that assigns participants to a tested intervention. The registered 162 participants enrollment target is mid-sized for trials with a published cap, below the 192-participant average among 14 other Labor Pain trials with a reported enrollment target (16% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Labor Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06498908's enrollment target sits among peer trials
162 6th of 14 higher than 9 of 14 other Labor Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Labor Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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