Comparing the effectiveness of copper intrauterine devices available in Canada. Is FlexiT non-inferior to NovaT when inserted immediately after first-trimester abortion? Study protocol for a randomized controlled trial

被引:1
|
作者
Norman, Wendy V. [1 ,2 ,3 ]
Chiles, Jessica L. [1 ,2 ]
Turner, Caroline A. [1 ,2 ]
Brant, Rollin [1 ,4 ]
Aslan, Andra [1 ,2 ]
Kaczorowski, Janusz [1 ,5 ]
机构
[1] Womens Hlth Res Inst, Contracept Access Res Team, Vancouver, BC V6H 1G3, Canada
[2] Univ British Columbia, Dept Family Practice, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, Dept Stat, Vancouver, BC V6H 3V4, Canada
[5] Univ Montreal, Dept Med Familiale & Med Urgence, Montreal, PQ, Canada
关键词
Contraception; Intrauterine device; Intrauterine device expulsion; Contraception effectiveness; Abortion-induced; Therapeutic abortion; Non-inferiority trial; Randomized controlled trial; Canada; CONTRACEPTIVE DEVICE; IUD-INSERTION; SATISFACTION; WOMEN;
D O I
10.1186/1745-6215-13-147
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: We describe the rationale and protocol for a randomized noninferiority controlled trial (RCT) to determine if the Flexi-T380(+) copper intrauterine contraceptive device (IUD) is comparable in terms of effectiveness and expulsion rates to the most common Canadian IUD currently in use, NovaT-200, when placed immediately after a first-trimester abortion. Methods/Design: Consenting women choosing to use an IUD after an abortion for a pregnancy of less than 12 weeks of gestation will be randomized to device-type groups to receive immediate post-abortion placement of either a Flexi-T380(+) IUD, a device for which no current evidence on expulsion or effectiveness rates is available, or the Nova-T200 IUD, the only other brand of copper IUD available in Canada at the time of study initiation. The primary outcome measure is IUD expulsion rate at 1 year. Secondary outcomes include: pregnancy rate, method continuation rate, complication rates (infection, perforation), and satisfaction with contraceptive method. A non-intervention group of consenting women choosing a range of other post-abortion contraception methods, including no contraception, will be included for comparison of secondary outcomes. Web-based contraception satisfaction questionnaires, clinical records, and government-linked health administrative databases will be used to assess primary and secondary outcomes. Discussion: The RCT design, combined with access to clinical records at all provincial abortion clinics, and to information in provincial single-payer linked administrative health databases, birth registry, and hospital records, offers a unique opportunity to determine if a novel IUD has a comparable expulsion rate to that of the current standard IUD in Canada, in addition to the first opportunity to determine pregnancy rate and method satisfaction at 1 year post-abortion for women choosing a range of post-abortion contraceptive options. We highlight considerations of design, implementation, and evaluation of the first trial to provide rigorous evidence for the effectiveness of current Canadian IUDs when inserted after first-trimester abortion.
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页数:6
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  • [1] Comparing the effectiveness of copper intrauterine devices available in Canada. Is FlexiT non-inferior to NovaT when inserted immediately after first-trimester abortion? Study protocol for a randomized controlled trial
    Wendy V Norman
    Jessica L Chiles
    Caroline A Turner
    Rollin Brant
    Andra Aslan
    Janusz Kaczorowski
    Trials, 13