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NCT01309919 · ClinicalTrials.gov registry record · NA
Bleeding Patterns and Complications After Postpartum IUD Placement: a Pilot Study
A NA study, sponsored by Baystate Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 150
- Enrollment target
NCT01309919 is a NA study that has completed, run by Baystate Medical Center. The registered enrollment target is 150 participants.
The verdict
NCT01309919, a NA study, has completed, sponsored by Baystate Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
Study Summary
The purpose of the study is to determine the feasibility of placing the levonorgestrel-releasing intrauterine system (LNG - IUS, Mirena®) post-delivery. The investigators will gain information about complications at the time of placement; the investigators will also examine the expulsion rate, side effects, bleeding patterns and subject satisfaction at various time periods after insertion.
Interventions
- OTHER Diary
- DEVICE IUD
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2011-01 |
| Est. Completion | 2012-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01309919
The ClinicalTrials.gov registry entry for NCT01309919 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baystate Medical Center, which has 36 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Diary is the first listed.
NCT01309919 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01309919 about?
NCT01309919 is a clinical study titled "Bleeding Patterns and Complications After Postpartum IUD Placement: a Pilot Study". The purpose of the study is to determine the feasibility of placing the levonorgestrel-releasing intrauterine system (LNG - IUS, Mirena®) post-delivery. The investigators will gain information about complications at the time of placement; the investigators will also examine the expulsion rate, side ...
What is the current status of trial NCT01309919?
This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2011-01. Estimated completion is 2012-02.
What interventions are being tested in trial NCT01309919?
The interventions under investigation include: Diary (OTHER), IUD (DEVICE).
Who is sponsoring clinical trial NCT01309919?
This trial is sponsored by Baystate Medical Center, which has 36 total clinical trials registered on ClinicalTrials.gov.
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