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A cross-sectional, observational multicenter study to assess the reasons for choosing the 3-year hormonal IUD and level of IUDs knowledge among women aged 18 to 29 years. The study will be conducted in standard clinical practice conditions at public and private gynecology clinics and during a single study visit.
Approximately 1,000 women aged 18 to 29 years who have freely chosen the 3 year hormonal IUD as their contraceptive method will be included in the study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| BAY86-5028 | Women aged 18 to 29 years that use Jaydess for contraception |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Levonorgestrel (Jaydess, Skyla, BAY86-5028) | Drug | Intrauterine delivery system Jaydess (13.5 mg levonorgestrel) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Reason for choosing Jaydess as intrauterine device (IUD) | The participants select the reason out of a given list of 15 possible reasons | day 1 |
| Reason for switching to Jaydess if used another type of intrauterine device before | The participants select the reason out of a given list of 10 possible reasons | day 1 |
| Knowledge of Jaydess or other IUDs prior to the visit | The participants select the reason out of a given list of 3 possible reasons | day 1 |
| Is the first intrauterine device prescribed? | Possible reasons: Yes or No | day 1 |
| Person who encouraged the use of jaydess? | The participants select the answer out of a given list of 5 possible people | day 1 |
| Measure | Description | Time Frame |
|---|---|---|
| Reason for not using Jaydess or other intrauterine delivery system (IUD) before | The participants select the reason out of a given list of 12 possible reasons | day 1 |
| Uterine length as measured by ultrasonography |
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Inclusion Criteria:
Exclusion Criteria:
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The study population will consist of women aged 18-29 years, who have freely chosen Jaydess for contraception after being adequately counseled and informed of all contraceptive options by their physician at a previous visit to the study visit in a routine clinical practice setting
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| Name | Affiliation | Role |
|---|---|---|
| Bayer Study Director | Bayer | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Multiple Locations | Spain |
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| day 1 |
| Presence of dysmenorrhea (Y/N) | day 1 |
| Current contraception method | The participants select out of a given list of 20 options | day 1 |
| Date of birth | day 1 |
| Marital status | day 1 |
| Place of birth | day 1 |
| Place of residence | day 1 |
| Educational level | day 1 |
| Employment | day 1 |
| Income level | day 1 |
| Do you have children? (Y/N) | day 1 |
| Number of children | day 1 |
| Has she had some birth vaginally? (Y/N) | day 1 |
| Date of last birth | day 1 |
| Do you plan to have (more) children? (Yes/No/Unknown) | day 1 |
| When she plans to have (more) children | day 1 |
| Frequency of menstrual bleeding | day 1 |
| Regularity of menstrual bleeding | day 1 |
| Quantity of menstrual bleeding | day 1 |
| Duration of menstrual bleeding | day 1 |
| Absence of menstrual bleeding | day 1 |
| Questionnaire concerning the physicians' characteristics | The questionnaire consists of 7 questions | day 1 |
| ID | Term |
|---|---|
| D016912 | Levonorgestrel |
| ID | Term |
|---|---|
| D009644 | Norgestrel |
| D009652 | Norpregnenes |
| D009650 | Norpregnanes |
| D009654 | Norsteroids |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |
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