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NCT06964373 · ClinicalTrials.gov registry record · NA
Cervical Ripening Balloons for Same-Day Cervical Prep
A NA study of Dilation and Evacuation, sponsored by University of New Mexi.
- Recruiting
- Registry status
- NA
- Development phase
- 70
- Enrollment target
- 1
- Study location
NCT06964373 is a NA study of Dilation and Evacuation that is actively recruiting participants, run by University of New Mexi. The registered enrollment target is 70 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06964373, a NA study of Dilation and Evacuation, is actively recruiting participants, sponsored by University of New Mexi.
- RECRUITING
- Registry status
- NA
- Development phase
- 70 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to learn if a cervical ripening balloon (Foley balloon) works to prepare the cervix before same-day outpatient dilation and evacuation (D\&E). The main questions it aims to answer are: * Is cervical preparation with cervical ripening balloon for same-day outpatient D\&E non-inferior to cervical preparation with osmotic dilators? * How feasible and safe is cervical preparation with cervical ripening balloon for same-day outpatient D\&E? * How acceptable is cervical preparation with cervical ripening balloon for same-day outpatient D\&E? Participants will: * Have cervical preparation with cervical ripening balloon (experimental group) or osmotic dilators (usual care group) * Complete two surveys, one about the cervical preparation and one about the D\&E procedure
Conditions Studied
Interventions
- DEVICE Osmotic Dilators
- DEVICE Cervical Ripening Balloon
Study Locations (1)
New Mexico
- University of New Mexico - Albuquerque
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70 participants |
| Start Date | 2025-04-08 |
| Est. Completion | 2026-07-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06964373
The ClinicalTrials.gov registry entry for NCT06964373 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of New Mexi, which has 76 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Dilation and Evacuation appearing as the primary indexed condition, and to 2 interventions - of which Osmotic Dilators is the first listed.
NCT06964373 reports 1 study location spanning 1 distinct geographic area - top geographies include New Mexico.
Frequently Asked Questions
What is clinical trial NCT06964373 about?
NCT06964373 is a clinical study titled "Cervical Ripening Balloons for Same-Day Cervical Prep". The goal of this clinical trial is to learn if a cervical ripening balloon (Foley balloon) works to prepare the cervix before same-day outpatient dilation and evacuation (D\&E). The main questions it aims to answer are: * Is cervical preparation with cervical ripening balloon for same-day outpatien...
What is the current status of trial NCT06964373?
This trial is currently recruiting. It is a NA study. The enrollment target is 70 participants. The study started on 2025-04-08. Estimated completion is 2026-07-31.
What conditions does trial NCT06964373 study?
This clinical trial studies the following conditions: Dilation and Evacuation.
What interventions are being tested in trial NCT06964373?
The interventions under investigation include: Osmotic Dilators (DEVICE), Cervical Ripening Balloon (DEVICE).
Who is sponsoring clinical trial NCT06964373?
This trial is sponsored by University of New Mexi, which has 76 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06964373 being conducted?
This trial has 1 study location across New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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