Evidence map›Paper›PMID 31231065›Full record

ArticleThe Lancet. Global health2019

Efficacy of the 1-year (13-cycle) segesterone acetate and ethinylestradiol contraceptive vaginal system: results of two multicentre, open-label, single-arm, phase 3 trials.

David F Archer, Ruth B Merkatz, Luis Bahamondes, Carolyn L Westhoff, Philip Darney, Dan Apter, Jeffrey T Jensen, Vivian Brache, Anita L Nelson, Erika Banks and 8 more

2 registry-linked trialsAbstract readMulticenter Study
In one paragraph

Article in The Lancet. Global health, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00263341 phase3completednot on this map

A Multicenter, Open-label Study on the Efficacy, Cycle Control and Safety of a Contraceptive Vaginal Ring Delivering a Daily Dose of 150 ug of Nestorone® and 15 ug of Ethinyl Estradiol

TypeinterventionalSponsorPopulation CouncilRan2005 to 2014Enrolled1,135ConditionsContraceptionArmsNES/EE CVR
NCT00455156 phase3completednot on this map

A Multicenter, Open-label Study on the Efficacy, Cycle Control and Safety of a Contraceptive Vaginal Ring Delivering a Daily Dose of 150µg of Nestorone® and 15µg of Ethinyl Estradiol (150/15 NES/EE CVR)

TypeinterventionalSponsorPremier ResearchRan2006 to 2011Enrolled1,200ConditionsContraceptionArms150 mg of Nestorone and 15 mg of ethinyl estradiol (150/15 NES/EE CVR)
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
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  7. Novel male contraceptives.Future science OA · 2026
    Review
  8. Article
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  11. Review
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  19. Review
  20. New Contraception Update - Annovera, Phexxi, Slynd, and Twirla.Current obstetrics and gynecology reports · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

David F ArcherClinical Research Center, Eastern Virginia Medical School, Norfolk, VA, USA.
Ruth B MerkatzCenter for Biomedical Research, Population Council, New York, NY, USA. Electronic address: rmerkatz@popcouncil.org.
Luis BahamondesFamily Planning Clinic, Department of Obstetrics and Gynecology, Faculty of Medical Sciences, University of Campinas, Campinas, São Paulo, Brazil.
Carolyn L WesthoffColumbia University, Irving Medical Center, New York, NY, USA.
Philip DarneyBixby Center for Global Reproductive Health, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, CA, USA.
Dan ApterVL-Medi Clinical Research Center, Helsinki, Finland.
Jeffrey T JensenDepartment of Obstetrics and Gynecology, Oregon Health & Science University, Portland, OR, USA.
Vivian BracheProfamilia, Biomedical Research Department, Santo Domingo, Dominican Republic.
Anita L NelsonResearch Division, Essential Access Health, Los Angeles, CA, USA.
Erika BanksDepartment of Obstetrics & Gynecology and Women's Health, Albert Einstein College of Medicine, Montefiore Medical Center, New York City, NY, USA.
György BártfaiDepartment of Obstetrics and Gynaecology, University of Szeged, Szeged, Hungary.
David J PortmanColumbus Center for Women's Health Research, Columbus, OH, USA; Sermonix Pharmaceuticals, Columbus, OH, USA.
Marlena PlagianosCenter for Biomedical Research, Population Council, New York, NY, USA.
Clint DartHealth Decisions, Durham, NC, USA.
Narender KumarCenter for Biomedical Research, Population Council, New York, NY, USA.
George W CreasyCenter for Biomedical Research, Population Council, New York, NY, USA.
Regine Sitruk-WareCenter for Biomedical Research, Population Council, New York, NY, USA.
Diana L BlitheContraception Research Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.

Funding

Development of novel contraceptive methods for men and womenZIBHD008987 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BLITHE, DIANA · 2019 to 2025
$7.2M
6 · The paper itself

Abstract

backgroundA ring-shaped, contraceptive vaginal system designed to last 1 year (13 cycles) delivers an average of 0·15 mg segesterone acetate and 0·013 mg ethinylestradiol per day. We evaluated the efficacy of this contraceptive vaginal system and return to menses or pregnancy after use.

methodsIn two identically designed, multicentre, open-label, single-arm, phase 3 trials (one at 15 US academic and community sites and one at 12 US and international academic and community sites), participants followed a 21-days-in, 7-days-out segesterone acetate and ethinylestradiol contraceptive vaginal system schedule for up to 13 cycles. Participants were healthy, sexually active, non-pregnant, non-sterilised women aged 18-40 years. Women were cautioned that any removals during the 21 days of cyclic use should not exceed 2 h, and used daily paper diaries to record vaginal system use. Consistent with regulatory requirements for contraceptives, we calculated the Pearl Index for women aged 35 years and younger, excluding adjunctive contraception cycles, as the primary efficacy outcome measure. We also did intention-to-treat Kaplan-Meier life table analyses and followed up women who did not use hormonal contraceptives or desired pregnancy after study completion for 6 months for return to menses or pregnancy. The trials are registered with ClinicalTrials.gov, numbers NCT00455156 and NCT00263341.

findingsBetween Dec 19, 2006, and Oct 9, 2009, at the 15 US sites, and between Nov 1, 2006, and July 2, 2009, at the 12 US and international sites we enrolled 2278 women. Our overall efficacy analysis included 2265 participants (1130 in the US study and 1135 in the international study) and 1303 (57·5%) participants completed up to 13 cycles. The Pearl Index for the primary efficacy group was 2·98 (95% CI 2·13-4·06) per 100 woman-years, and was well within the range indicative of efficacy for a contraceptive under a woman's control. The Kaplan-Meier analysis revealed the contraceptive vaginal system was 97·5% effective, which provided further evidence of efficacy. Pregnancy occurrence was similar across cycles. All 290 follow-up participants reported return to menses or became pregnant (24 [63%] of 38 women who desired pregnancy) within 6 months.

interpretationThe segesterone acetate and ethinylestradiol contraceptive vaginal system is an effective contraceptive for 13 consecutive cycles of use. This new product adds to the contraceptive method mix and the 1-year duration of use means that women do not need to return to the clinic or pharmacy for refills every few months.

fundingEunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health, the US Agency for International Development, and the WHO Reproductive Health Research Department.

Indexed as

Clinical Trials, Phase III as TopicContraceptive Devices, FemaleEthinyl EstradiolInfusion Pumps, ImplantableOutcome Assessment, Health CarePregnenedionesAdolescentAdultDrug CombinationsFemaleHumansTreatment OutcomeYoung AdultDrug CombinationsEthinyl EstradiolPregnenedionessegesterone acetate and ethinyl estradiol vaginal system

Identifiers

PMID31231065
PMCPMC6624423

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.