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NCT06799052 · ClinicalTrials.gov registry record · NA
Cervical Preparation for Same-Day Dilation & Evacuation
A NA study of Procedural Pain and Abortion, Second Trimester, sponsored by Boston Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 32
- Enrollment target
- 1
- Study location
NCT06799052 is a NA study of Procedural Pain and Abortion, Second Trimester that is actively recruiting participants, run by Boston Medical Center. The registered enrollment target is 32 participants, below the 58-participant average among 9 other Procedural Pain trials with a reported enrollment target (45% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06799052, a NA study of Procedural Pain and Abortion, Second Trimester, is actively recruiting participants, sponsored by Boston Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 32 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a noninferiority randomized control trial of two cervical preparation methods prior to same-day Dilation \& Evacuation (D\&E). Cervical preparation is a process that softens and dilates the cervix prior to a procedure. The primary objective is to evidence noninferiority of cervical preparation using a single-balloon catheter method when compared to a group receiving osmotic dilators, specifically in D\&E operative time. Secondary objectives will compare the two methods for adequate dilation, ability to complete the operation in the same day, participant pain, satisfaction and safety.
Conditions Studied
Interventions
- DEVICE Transcervical single-balloon catheter
- DEVICE Synthetic osmotic dilators
Study Locations (1)
Massachusetts
- Boston Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2025-06-12 |
| Est. Completion | 2026-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06799052
The ClinicalTrials.gov registry entry for NCT06799052 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 58-participant average among 9 other Procedural Pain trials with a reported enrollment target (45% lower). The listed sponsor is Boston Medical Center, which has 253 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Procedural Pain appearing as the primary indexed condition, and to 2 interventions - of which Transcervical single-balloon catheter is the first listed.
NCT06799052 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT06799052 about?
NCT06799052 is a clinical study titled "Cervical Preparation for Same-Day Dilation & Evacuation". This is a noninferiority randomized control trial of two cervical preparation methods prior to same-day Dilation \& Evacuation (D\&E). Cervical preparation is a process that softens and dilates the cervix prior to a procedure. The primary objective is to evidence noninferiority of cervical preparat...
What is the current status of trial NCT06799052?
This trial is currently recruiting. It is a NA study. The enrollment target is 32 participants. The study started on 2025-06-12. Estimated completion is 2026-09.
What conditions does trial NCT06799052 study?
This clinical trial studies the following conditions: Procedural Pain, Abortion, Second Trimester, Procedural Complication.
What interventions are being tested in trial NCT06799052?
The interventions under investigation include: Transcervical single-balloon catheter (DEVICE), Synthetic osmotic dilators (DEVICE).
Who is sponsoring clinical trial NCT06799052?
This trial is sponsored by Boston Medical Center, which has 253 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06799052 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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