Trials / Completed
CompletedNCT03074903
Does Skyla Insertion Timing Impact Bleeding?
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 132 (actual)
- Sponsor
- Rutgers, The State University of New Jersey · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
Women presenting for contraception will be offered the IUS Skyla and study participation. Daily bleeding will be collected for a total of 90 days and correlated with insertion timing and baseline endometrial thickness.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Intrauterine system | Women having the Skyla intrauterine system at different times during their menstrual cycle report their bleeding patterns through daily texts. |
Timeline
- Start date
- 2016-04-16
- Primary completion
- 2017-07-27
- Completion
- 2017-07-28
- First posted
- 2017-03-09
- Last updated
- 2018-02-13
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03074903. Inclusion in this directory is not an endorsement.