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NCT02033083 · ClinicalTrials.gov registry record · NA
Laminaria Compared to Dilapan-S for Cervical Preparation Before Dilation and Evacuation at 18-24 Weeks of Gestation
A NA study of Second Trimester Abortion, sponsored by Planned Parenthood of Greater New York.
- Completed
- Registry status
- NA
- Development phase
- 180
- Enrollment target
- 1
- Study location
NCT02033083 is a NA study of Second Trimester Abortion that has completed, run by Planned Parenthood of Greater New York. The registered enrollment target is 180 participants. The trial reports 1 study location across 1 state.
The verdict
NCT02033083, a NA study of Second Trimester Abortion, has completed, sponsored by Planned Parenthood of Greater New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 180 participants
- Enrollment target
- 1
- Study location
Study Summary
Primary objective: To study the difference in dilation and evacuation (D\&E) procedure time following overnight cervical preparation with laminaria or Dilapan-S™. The investigators hypothesize procedure time will be less with Dilapan-S™. Secondary objectives: To compare the use of laminaria and Dilapan-S™ for differences in: (1) initial cervical dilation before D\&E; (2) need for mechanical dilation to accomplish D\&E and ease of dilation if required; (3) number of osmotic dilators placed; (4) ability to complete the D\&E procedure without further cervical preparation; (5) complications; (6) pain and other side effects; (7) patient acceptability; and (8) provider acceptability.
Conditions Studied
Interventions
- DEVICE Dilapan-S
- DEVICE Laminaria
Study Locations (1)
New York
- Planned Parenthood of New York City - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 180 participants |
| Start Date | 2013-12 |
| Est. Completion | 2016-02 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02033083
The ClinicalTrials.gov registry entry for NCT02033083 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 180 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 1 condition, with Second Trimester Abortion appearing as the primary indexed condition, and to 2 interventions - of which Dilapan-S is the first listed.
NCT02033083 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT02033083 about?
NCT02033083 is a clinical study titled "Laminaria Compared to Dilapan-S for Cervical Preparation Before Dilation and Evacuation at 18-24 Weeks of Gestation". Primary objective: To study the difference in dilation and evacuation (D\&E) procedure time following overnight cervical preparation with laminaria or Dilapan-S™. The investigators hypothesize procedure time will be less with Dilapan-S™. Secondary objectives: To compare the use of laminaria and Dil...
What is the current status of trial NCT02033083?
This trial is currently completed. It is a NA study. The enrollment target is 180 participants. The study started on 2013-12. Estimated completion is 2016-02.
What conditions does trial NCT02033083 study?
This clinical trial studies the following conditions: Second Trimester Abortion.
What interventions are being tested in trial NCT02033083?
The interventions under investigation include: Dilapan-S (DEVICE), Laminaria (DEVICE).
Who is sponsoring clinical trial NCT02033083?
This trial is sponsored by Planned Parenthood of Greater New York, which has 6 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02033083 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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