CLINICAL TRIALS PROFILE FOR NUVARING
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All Clinical Trials for NUVARING
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT00269620 ↗ | PARIS or PAtch RIng Study: A Trial to Evaluate NuvaRing Versus OrthoEvra | Completed | Magee-Womens Hospital | Phase 4 | 2005-06-01 | This is an open-label prospective, multicenter, randomized trial to compare continuation rates into the fourth cycle of women using either the NuvaRing or OrthoEvra. Five hundred women will be recruited at 9 centers nationwide to be randomly assigned to use either the NuvaRing or OrthoEvra for four months. Women must either be on the pill or have recently stopped the pill and be relatively satisfied with oral contraceptive use to qualify for enrollment. Two visits and two phone calls will be required. |
NCT00269620 ↗ | PARIS or PAtch RIng Study: A Trial to Evaluate NuvaRing Versus OrthoEvra | Completed | Organon | Phase 4 | 2005-06-01 | This is an open-label prospective, multicenter, randomized trial to compare continuation rates into the fourth cycle of women using either the NuvaRing or OrthoEvra. Five hundred women will be recruited at 9 centers nationwide to be randomly assigned to use either the NuvaRing or OrthoEvra for four months. Women must either be on the pill or have recently stopped the pill and be relatively satisfied with oral contraceptive use to qualify for enrollment. Two visits and two phone calls will be required. |
NCT00269620 ↗ | PARIS or PAtch RIng Study: A Trial to Evaluate NuvaRing Versus OrthoEvra | Completed | University of Pittsburgh | Phase 4 | 2005-06-01 | This is an open-label prospective, multicenter, randomized trial to compare continuation rates into the fourth cycle of women using either the NuvaRing or OrthoEvra. Five hundred women will be recruited at 9 centers nationwide to be randomly assigned to use either the NuvaRing or OrthoEvra for four months. Women must either be on the pill or have recently stopped the pill and be relatively satisfied with oral contraceptive use to qualify for enrollment. Two visits and two phone calls will be required. |
NCT00357526 ↗ | Oral Contraceptive Pills Compared to Vaginal Rings | Completed | Organon | N/A | 2003-04-01 | The purpose of this study is to determine whether teens and young women would prefer the Nuvaring to oral contraceptive pills after having tried both methods. |
NCT00357526 ↗ | Oral Contraceptive Pills Compared to Vaginal Rings | Completed | University of California, San Francisco | N/A | 2003-04-01 | The purpose of this study is to determine whether teens and young women would prefer the Nuvaring to oral contraceptive pills after having tried both methods. |
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. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for NUVARING
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