Status:
COMPLETED
LCS12 vs Combined Oral Contraceptive (COC) User Satisfaction Study
Lead Sponsor:
Bayer
Conditions:
Contraception
Eligibility:
FEMALE
18-29 years
Phase:
PHASE3
Brief Summary
The primary objective of this study is to evaluate user satisfaction and tolerability in young women (18-29 years of age) using the LCS12 compared with young women using a COC (Yasmin) over a period o...
Eligibility Criteria
Inclusion
- Subject has signed and dated the Informed Consent Form (ICF).
- The subject is generally healthy, requesting contraception, and is between 18 and 29 years of age (inclusive) at Screening.
- In the opinion of the investigator, the subject is
- in good health;
- without uterine conditions that would preempt insertion of LCS12;
- without conditions/history that would contraindicate the use of oral contraceptives.
- Subject has normal or clinically insignificant cervical smear (ie, one that does not require further follow up). A cervical smear must be taken at the Screening Visit or a documented normal result has to have been obtained within 6 months of Screening. Subjects with atypical squamous cells of undetermined significance (ASCUS) can be included in the study if they have a Human Papilloma Virus (HPV) deoxyribonucleic acid (DNA) test that, according to the standards of the local laboratory, is negative for high-risk HPV.
- As determined by subject's history, subject has regular (ie, endogenous cyclicity without hormonal contraceptive use) menstrual cycles (length of cycle 21-35 days).
- Subject is willing and able to attend the scheduled study visits and to comply with the study procedures.
Exclusion
- Pregnancy or current lactation (less than 6 weeks since vaginal or Cesarean delivery or abortion). Note: Postpartum LCS12 insertions should be postponed until the uterus is fully involuted, and not earlier than 6 weeks after delivery. If involution is substantially delayed, the investigator should consider waiting until 12 weeks postpartum.
- Infected abortion or postpartum endometritis within 3 months prior to the Screening Visit (Visit 1)
- Chronic, daily use of drugs that may increase serum potassium levels, such as nonsteroidal anti-inflammatory drugs (NSAIDs, eg. ibuprofen and naproxen), potassium-sparing diuretics (eg. spironolactone), potassium supplementation, angiotensin converting enzyme (ACE) inhibitors, angiotensin-II receptor antagonists, aldosterone antagonists, and heparin.
- Abnormal uterine bleeding of unknown origin/undiagnosed abnormal genital bleeding
- Any genital infection (until successfully treated)
- Abnormal cervical smear result (see inclusion criteria)
- Acute, current or history of recurrent pelvic inflammatory disease
- Congenital or acquired uterine anomaly or any distortion of the uterine cavity (eg, by fibroids) that, in the opinion of the investigator, would cause problems during insertion, retention, or removal of LCS12.
Key Trial Info
Start Date :
January 6 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 28 2014
Estimated Enrollment :
567 Patients enrolled
Trial Details
Trial ID
NCT01254292
Start Date
January 6 2011
End Date
May 28 2014
Last Update
September 25 2017
Active Locations (94)
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1
Visions Clinical Research - Tucson
Tucson, Arizona, United States, 85712
2
Tucson, Arizona, United States, 85712
3
Grossmont Center for Clinical Research
La Mesa, California, United States, 91942
4
La Mesa, California, United States, 91942