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NCT00775983 · ClinicalTrials.gov registry record · NA
Dilapan Versus Laminaria
A NA study of Cervical Preparation, sponsored by University of California, San Francisco.
- Completed
- Registry status
- NA
- Development phase
- 72
- Enrollment target
- 1
- Study location
NCT00775983 is a NA study of Cervical Preparation that has completed, run by University of California, San Francisco. The registered enrollment target is 72 participants. The trial reports 1 study location across 1 state.
The verdict
NCT00775983, a NA study of Cervical Preparation, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- NA
- Development phase
- 72 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a randomized, blinded clinical trial comparing overnight laminaria versus same-day Dilapan for cervical preparation for surgical abortions occurring between fourteen and eighteen weeks gestation. Comparisons will be made between procedure time, need for additional dilation, occurrence of complications, and patient and provider satisfaction. Hypothesis: Cervical preparation for surgical abortion, between fourteen and eighteen weeks gestation, with same-day Dilapan is non-inferior to cervical preparation with overnight laminaria within a five-minute difference. Primary objective: Determine differences in procedure times Secondary objectives: Examine complications, and need for additional dilation between early second-trimester surgical abortions performed after cervical preparation with same-day Dilapan versus those performed after cervical preparation with overnight laminaria
Conditions Studied
Interventions
- DEVICE Dilapan-S
- DEVICE laminaria
Study Locations (1)
California
- San Francisco General Hospital - San Francisco
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2008-10 |
| Est. Completion | 2009-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00775983
The ClinicalTrials.gov registry entry for NCT00775983 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Cervical Preparation appearing as the primary indexed condition, and to 2 interventions - of which Dilapan-S is the first listed.
NCT00775983 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT00775983 about?
NCT00775983 is a clinical study titled "Dilapan Versus Laminaria". This is a randomized, blinded clinical trial comparing overnight laminaria versus same-day Dilapan for cervical preparation for surgical abortions occurring between fourteen and eighteen weeks gestation. Comparisons will be made between procedure time, need for additional dilation, occurrence of com...
What is the current status of trial NCT00775983?
This trial is currently completed. It is a NA study. The enrollment target is 72 participants. The study started on 2008-10. Estimated completion is 2009-12.
What conditions does trial NCT00775983 study?
This clinical trial studies the following conditions: Cervical Preparation.
What interventions are being tested in trial NCT00775983?
The interventions under investigation include: Dilapan-S (DEVICE), laminaria (DEVICE).
Who is sponsoring clinical trial NCT00775983?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00775983 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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