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NCT02311478 · ClinicalTrials.gov registry record · NA
Tracking IUD Bleeding Experiences: An Evaluation of Bleeding Profiles in New Intrauterine Device Users
A NA study, sponsored by University of Utah.
- Completed
- Registry status
- NA
- Development phase
- 79
- Enrollment target
NCT02311478: Completed NA study, sponsored by University of Utah.
NCT02311478 is a NA study that has completed, run by University of Utah. The registered enrollment target is 79 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02311478, a NA study, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- NA
- Development phase
- 79 participants
- Enrollment target
Study Summary
This study aims to use validated tools as well as new technology to examine changes in bleeding patterns among women who are initiating the copper T380A IUD.
Primary Outcome
Evaluate bleeding duration among women initiating the copper T380 IUD during the 90 days prior to initiation compared to two 90 periods after IUD insertion. Women will track bleeding after the insertion of the T380A IUD for 180 days. Participants will be contacted monthly to collect data.
Interventions
- DEVICE T380A Intrauterine Copper Contraceptive
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 79 participants |
| Start Date | 2014-12 |
| Est. Completion | 2017-02 |
| Phase | NA |
What the finished NCT02311478 record still lists
NCT02311478 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 79 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).
The record links to 0 conditions, and to 1 intervention - of which T380A Intrauterine Copper Contraceptive is the first listed.
NCT02311478 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02311478 about?
NCT02311478 is a clinical study titled "Tracking IUD Bleeding Experiences: An Evaluation of Bleeding Profiles in New Intrauterine Device Users". This study aims to use validated tools as well as new technology to examine changes in bleeding patterns among women who are initiating the copper T380A IUD.
What is the current status of trial NCT02311478?
This trial is currently completed. It is a NA study. The enrollment target is 79 participants. The study started on 2014-12. Estimated completion is 2017-02.
What interventions are being tested in trial NCT02311478?
The interventions under investigation include: T380A Intrauterine Copper Contraceptive (DEVICE).
Who is sponsoring clinical trial NCT02311478?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02311478's enrollment target sits among peer trials
79 1060th of 2000 higher than 941 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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