CLINICAL TRIALS PROFILE FOR ETHINYL ESTRADIOL; ETONOGESTREL
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All Clinical Trials for ethinyl estradiol; etonogestrel
| Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
|---|---|---|---|---|---|---|
| NCT00369967 ↗ | Quick Start Initiation of the Contraceptive Vaginal Ring in Adolescents | Terminated | American College of Obstetricians and Gynecologists | N/A | 2007-02-01 | We hypothesize that using "quick start" initiation of the contraceptive vaginal ring in adolescents seeking birth control will improve compliance compared to traditional start. We will conduct a randomized controlled trial comparing "quick start" to traditional start initiation of the contraceptive vaginal ring in adolescents seeking birth control. The primary study outcome is method continuation at 3, 6, and 12 months. Secondary outcomes include abnormal bleeding, product satisfaction, and adverse events. |
| NCT00369967 ↗ | Quick Start Initiation of the Contraceptive Vaginal Ring in Adolescents | Terminated | Bayer | N/A | 2007-02-01 | We hypothesize that using "quick start" initiation of the contraceptive vaginal ring in adolescents seeking birth control will improve compliance compared to traditional start. We will conduct a randomized controlled trial comparing "quick start" to traditional start initiation of the contraceptive vaginal ring in adolescents seeking birth control. The primary study outcome is method continuation at 3, 6, and 12 months. Secondary outcomes include abnormal bleeding, product satisfaction, and adverse events. |
| NCT00369967 ↗ | Quick Start Initiation of the Contraceptive Vaginal Ring in Adolescents | Terminated | Virginia Commonwealth University | N/A | 2007-02-01 | We hypothesize that using "quick start" initiation of the contraceptive vaginal ring in adolescents seeking birth control will improve compliance compared to traditional start. We will conduct a randomized controlled trial comparing "quick start" to traditional start initiation of the contraceptive vaginal ring in adolescents seeking birth control. The primary study outcome is method continuation at 3, 6, and 12 months. Secondary outcomes include abnormal bleeding, product satisfaction, and adverse events. |
| NCT00612508 ↗ | Hormonal Contraception and Vaginal Health | Completed | Oregon Clinical and Translational Research Institute | N/A | 2007-05-01 | The purpose of this study is to help determine if the route by which women receive hormonal contraception causes different changes to occur in the lining of the vagina. The investigators plan to compare an oral route (taking birth control pills) with a vaginal route (using a vaginal ring). |
| NCT00612508 ↗ | Hormonal Contraception and Vaginal Health | Completed | Oregon Health and Science University | N/A | 2007-05-01 | The purpose of this study is to help determine if the route by which women receive hormonal contraception causes different changes to occur in the lining of the vagina. The investigators plan to compare an oral route (taking birth control pills) with a vaginal route (using a vaginal ring). |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for ethinyl estradiol; etonogestrel
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