Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT05700812 · ClinicalTrials.gov registry record · NA
IUD Placement Without Sounding
A NA study, sponsored by University of California, Davis.
- Completed
- Registry status
- NA
- Development phase
- 90
- Enrollment target
NCT05700812 is a NA study that has completed, run by University of California, Davis. The registered enrollment target is 90 participants.
The verdict
NCT05700812, a NA study, has completed, sponsored by University of California, Davis.
- COMPLETED
- Registry status
- NA
- Development phase
- 90 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the feasibility of a uterine sound sparing technique for levonorgestrel 52 mg intrauterine device (IUD) placement. This study will be conducted in three phases. In phase one, the IUD will be placed in standard fashion with a uterine sound to obtain baseline data. Phase two and three are interventional phases that will investigate IUD placement without the use of a uterine sound. In phase two, the IUD will be placed without the use of a uterine sound, but under abdominal ultrasound guidance. In phase three, the IUD will be placed without the use of a uterine sound and without ultrasound guidance. An ultrasound exam will be completed at the end of phase two and three to determine if the IUD was successful placed. To answer the secondary objectives, for all study phases the investigators will measure the procedure time, the participant-reported maximum pain during and 5-minutes post placement and the provider assessment of ease of placement. To determine the exploratory objective of IUD expulsion and perforation rate for a uterine sound sparing IUD placement technique, participants in phases two and three will complete a 30-day phone follow up and 90-day in clinic follow up to evaluate for IUD expulsion or perforation. The investigators hypothesize that the levonorgestrel 52 mg IUD can successfully be inserted without uterine sounding.
Interventions
- PROCEDURE Sound sparing levonorgestrel 52 mg IUD placement
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2023-02-01 |
| Est. Completion | 2024-07-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05700812
The ClinicalTrials.gov registry entry for NCT05700812 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Davis, which has 657 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Sound sparing levonorgestrel 52 mg IUD placement is the first listed.
NCT05700812 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT05700812 about?
NCT05700812 is a clinical study titled "IUD Placement Without Sounding". The purpose of this study is to determine the feasibility of a uterine sound sparing technique for levonorgestrel 52 mg intrauterine device (IUD) placement. This study will be conducted in three phases. In phase one, the IUD will be placed in standard fashion with a uterine sound to obtain baseline ...
What is the current status of trial NCT05700812?
This trial is currently completed. It is a NA study. The enrollment target is 90 participants. The study started on 2023-02-01. Estimated completion is 2024-07-31.
What interventions are being tested in trial NCT05700812?
The interventions under investigation include: Sound sparing levonorgestrel 52 mg IUD placement (PROCEDURE).
Who is sponsoring clinical trial NCT05700812?
This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.