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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: Completed NA study, sponsored by Baystate Medical Center.
NCT01309919 is a NA study that has completed, run by Baystate Medical Center. The registered enrollment target is 150 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Number of bleeding and spotting days in the first six weeks and subsequent six weeks postpartum
Interventions
- OTHER Diary
- DEVICE IUD
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2011-01 |
| Est. Completion | 2012-02 |
| Phase | NA |
What the finished NCT01309919 record still lists
NCT01309919 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower).
The record links to 0 conditions, and to 2 interventions - of which Diary is the first listed.
NCT01309919 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01309919's enrollment target sits among peer trials
150 661st of 2000 higher than 1,299 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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