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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02903888
Other study ID # 18883
Secondary ID
Status Completed
Phase N/A
First received September 13, 2016
Last updated January 10, 2018
Start date September 8, 2016
Est. completion date December 23, 2017

Study information

Verified date January 2018
Source Bayer
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 886
Est. completion date December 23, 2017
Est. primary completion date October 30, 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 29 Years
Eligibility Inclusion Criteria:

- Women aged 18 to 29 years.

- Women who decided to initiate treatment with a 3-year hormonal IUD for contraception after being adequately counseled and informed of all contraceptive options by their physician during a routine clinical visit, prior to the study visit (insertion visit).

- Women capable of reading and writing.

- Women who signed informed consent.

Exclusion Criteria:

- Women currently participating in an interventional clinical trial.

- Prescription of the 3-year hormonal IUD for non-contraceptive medical reasons.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Levonorgestrel (Jaydess, Skyla, BAY86-5028)
Intrauterine delivery system Jaydess (13.5 mg levonorgestrel)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Bayer

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reason for choosing Jaydess as intrauterine device (IUD) The participants select the reason out of a given list of 15 possible reasons day 1
Primary 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
Primary 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
Primary Is the first intrauterine device prescribed? Possible reasons: Yes or No day 1
Primary Person who encouraged the use of jaydess? The participants select the answer out of a given list of 5 possible people day 1
Secondary 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
Secondary Uterine length as measured by ultrasonography day 1
Secondary Presence of dysmenorrhea (Y/N) day 1
Secondary Current contraception method The participants select out of a given list of 20 options day 1
Secondary Date of birth day 1
Secondary Marital status day 1
Secondary Place of birth day 1
Secondary Place of residence day 1
Secondary Educational level day 1
Secondary Employment day 1
Secondary Income level day 1
Secondary Do you have children? (Y/N) day 1
Secondary Number of children day 1
Secondary Has she had some birth vaginally? (Y/N) day 1
Secondary Date of last birth day 1
Secondary Do you plan to have (more) children? (Yes/No/Unknown) day 1
Secondary When she plans to have (more) children day 1
Secondary Frequency of menstrual bleeding day 1
Secondary Regularity of menstrual bleeding day 1
Secondary Quantity of menstrual bleeding day 1
Secondary Duration of menstrual bleeding day 1
Secondary Absence of menstrual bleeding day 1
Secondary Questionnaire concerning the physicians' characteristics The questionnaire consists of 7 questions day 1