Background: The objective of this study was to compare cycle control, cycle-related characteristics and bodyweight effects of NuvaRing with those of a combined oral contraceptive (COC) containing 30 μg of ethinyl estradiol and 3 mg of drospirenone. Methods: A randomized, multicentre, open-label trial in which 983 women were treated (intent-to-treat population) with NuvaRing or the COC for 13 cycles. Results: Breakthrough bleeding or spotting during cycles 2-1 3 was in general less frequent with NuvaRing than that with the COC (4.7-10.4%) and showed a statistically significant odds ratio of 0.61 (95% confidence interval: 0.46, 0.80) with longitudinal analysis. Intended bleeding was significantly better for all cycles with NuvaRing (55.2-68.5%) than that with the COC (35.6-56.6%) (P < 0.01). Changes from baseline in mean bodyweight and body composition parameters were relatively small for both groups with no notable between-group differences. Conclusion: NuvaRing was associated with better cycle control than the COC, and there was no clinically relevant difference between the two groups in bodyweight. © 2006 Oxford University Press.
CITATION STYLE
Milsom, I., Lete, I., Bjertnaes, A., Rokstad, K., Lindh, I., Gruber, C. J., … Bastianelli, C. (2006). Effects on cycle control and bodyweight of the combined contraceptive ring, NuvaRing, versus an oral contraceptive containing 30 μg ethinyl estradiol and 3 mg drospirenone. Human Reproduction, 21(9), 2304–2311. https://doi.org/10.1093/humrep/del162
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