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NCT03002441 · ClinicalTrials.gov registry record · NA
Same-day Cervical Preparation Before Dilation and Evacuation
A NA study, sponsored by Planned Parenthood of Greater New York.
- Completed
- Registry status
- NA
- Development phase
- 54
- Enrollment target
NCT03002441 is a NA study that has completed, run by Planned Parenthood of Greater New York. The registered enrollment target is 54 participants.
The verdict
NCT03002441, a NA study, has completed, sponsored by Planned Parenthood of Greater New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 54 participants
- Enrollment target
Study Summary
The purpose of this randomized trial is to compare same-day cervical preparation using Dilapan-S™ plus buccal misoprostol to overnight cervical preparation using Dilapan-S™ before D\&E at 16.0 to 20.0 weeks. Primary objective: To compare D\&E operative time. We hypothesize that same-day Dilapan-S™ plus buccal misoprostol is non-inferior to overnight Dilapan-S™ with respect to operative time. Secondary objectives: To compare treatment groups for the following: Pre-operative cervical dilation; need for mechanical dilation and ease of dilation if required; ability to complete D\&E without further cervical preparation; ease of D\&E; complications; pain; side effects; patient and provider satisfaction.
Interventions
- DEVICE Same-Day Dilapan-S
- DEVICE Overnight Dilapan-S
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 54 participants |
| Start Date | 2016-12 |
| Est. Completion | 2020-02-28 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03002441
The ClinicalTrials.gov registry entry for NCT03002441 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Planned Parenthood of Greater New York, which has 6 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Same-Day Dilapan-S is the first listed.
NCT03002441 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03002441 about?
NCT03002441 is a clinical study titled "Same-day Cervical Preparation Before Dilation and Evacuation". The purpose of this randomized trial is to compare same-day cervical preparation using Dilapan-S™ plus buccal misoprostol to overnight cervical preparation using Dilapan-S™ before D\&E at 16.0 to 20.0 weeks. Primary objective: To compare D\&E operative time. We hypothesize that same-day Dilapan-S™ ...
What is the current status of trial NCT03002441?
This trial is currently completed. It is a NA study. The enrollment target is 54 participants. The study started on 2016-12. Estimated completion is 2020-02-28.
What interventions are being tested in trial NCT03002441?
The interventions under investigation include: Same-Day Dilapan-S (DEVICE), Overnight Dilapan-S (DEVICE).
Who is sponsoring clinical trial NCT03002441?
This trial is sponsored by Planned Parenthood of Greater New York, which has 6 total clinical trials registered on ClinicalTrials.gov.
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