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Article info
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Footnotes
ClinicalTrials.gov Identifier: NCT02175030
☆Conflicts of interest: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this article
☆☆Funding: This project is funded by the Eunice Kennedy Shriver National Institute of Child Health and Development (1R01HD083340). Additional support came by the University of Utah Population Health Research (PHR) Foundation, with funding in part from the National Center for Research Resources and the National Center for Advancing Translational Sciences (NCATS), National Institutes of Health (NIH), through Grant UL1TR002538 (formerly 5UL1TR001067-05, 8UL1TR000105 and UL1RR025764). Use of REDCap was provided by 8UL1TR000105 (formerly UL1RR025764) NCATS/NIH. DT and KF receive support from the Eunice Kennedy Shriver National Institute of Child Health & Human Development (DT K24HD087436, KF K12HD103096). The content is solely the responsibility of the authors and does not necessarily represent the official view of any of the funding agencies or participating institutions, including the National Institutes of Health, the University of Utah, or Planned Parenthood Federation of America, Inc. The funding sources had no role in study design, data collection, data analysis, manuscript writing, or the decision to publish.
☆☆The Division of Family Planning in the University of Utah's Department of Obstetrics and Gynecology receives research funding from Bayer Women's Health Care, Merck & Co. Inc., Cooper Surgical, Sebela Pharmaceuticals, Femasys, and Medicines 360. Rebecca Simmons did a short 1-week consultancy with a fertility tech company in January of 2020 for which she received compensation. DT serves as a consultant for Sebela Pharmaceuticals and the national principal investigator for FDA trials of two IUDs. The other authors did not report any potential conflicts of interest
☆☆Each author has confirmed compliance with the journal's requirements for authorship.