Trials / Unknown
UnknownNCT02021097
Study Evaluating Levonorgestrel and Ethinyl Estradiol for Oral Contraception
A Multicenter, Randomized, Open-labe, Controlled Study to Evaluate the Efficacy and Safety of the Combined Levonorgestrel(LNG) 100mcg and Ethinyl Estradiol(EE) 20mcg for Oral Contraception
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 1,008 (estimated)
- Sponsor
- Regenex Pharmaceutical, China · Academic / Other
- Sex
- Female
- Age
- 20 Years – 35 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the contraceptive efficacy and safety of an oral contraceptive containing a combination of LNG 100mcg/EE 20mcg compared to LNG 150mcg/EE 30 mcg.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Levonorgestrel 100 mcg and Ethinyl Estradiol 20 mcg | Tablet, orally, opd |
| DRUG | Levonorgestrel 150 mcg and Ethinyl Estradiol 30 mcg | Tablet, orally, opd |
Timeline
- Start date
- 2012-02-01
- Primary completion
- 2015-02-01
- Completion
- 2016-02-01
- First posted
- 2013-12-27
- Last updated
- 2013-12-27
Locations
21 sites across 1 country: China
Source: ClinicalTrials.gov record NCT02021097. Inclusion in this directory is not an endorsement.