Evidence map›Paper›PMID 20966692›Full record

Trial reportObstetrics and gynecology2010

Postplacental or delayed insertion of the levonorgestrel intrauterine device after vaginal delivery: a randomized controlled trial.

Beatrice A Chen, Matthew F Reeves, Jennifer L Hayes, Heather L Hohmann, Lisa K Perriera, Mitchell D Creinin

6 registry-linked trialsOpen access · greenAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Obstetrics and gynecology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 6 registered trials, which are not on this map. Cited by 49 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 8 pooled it
10.0field-weighted citation impact, top 2% of its field
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.

NCT00476021 nacompletednot on this map

Randomized Trial of Postplacental or Delayed Insertion of the Levonorgestrel-releasing Intrauterine Device After Vaginal Delivery

TypeinterventionalSponsorUniversity of PittsburghRan2007 to 2008Enrolled168ConditionsContraceptionArmsLevonorgestrel-releasing IUD (Mirena)
NCT01272960 nacompletednot on this map

Randomized, Open-label, Controlled Trial of Immediate Postpartum Versus Interval Insertion of Mirena to Increase the Usage at 6 Months After Delivery

TypeinterventionalSponsorWashington University School of MedicineRan2010 to 2012Enrolled53ConditionsPostpartum PeriodArmsPost-Placenta Mirena Insertion, Interval Insertion
NCT02067663 completednot on this mapstarted 2014, after this paper: background citation

Comparison of the Levonorgestrel IUD and the Copper IUD Placed in the Immediate Postplacental Period: A Prospective Cohort Study

TypeobservationalSponsorUniversity of Colorado, DenverRan2014 to 2015Enrolled123ConditionsContraceptionArmsParagard, Mirena
NCT02718222 nacompletednot on this mapstarted 2015, after this paper: background citation

Studying the Impact and Performance of Institutionalizing Immediate Post-partum IUD Services as a Routine Part of Antenatal Counseling and Delivery Room Services in Nepal, Sri Lanka, Tanzania

TypeinterventionalSponsorHarvard School of Public Health (HSPH)Ran2015 to 2018Enrolled140,258ConditionsContraceptionArmsPost-partum IUD
NCT03305081 naterminatednot on this mapstarted 2014, after this paper: background citation

Patient Compliance With Long-Acting Reversible Contraception Administration Immediately and Early Postpartum Versus Interval Postpartum

TypeinterventionalSponsorTulane University School of MedicineRan2014 to 2016Enrolled45ConditionsContraceptionArmsLevonorgestrel IUD, copper IUD, etonorgestrel implant
NCT03724708 naunknown statusnot on this mapstarted 2018, after this paper: background citation

Comparing Expulsion Rates When Using "Hang Up" Intrauterine Device Insertion Technique to Postplacental and Postpartum Insertion

TypeinterventionalSponsorKasr El Aini HospitalRan2018 to 2019Enrolled162ConditionsIUD Insertion Complication, IUD, Complications, Infection or InflammationArmsIUD
3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 8 syntheses or guidelines pooled it, 175 citations in OpenAlex.

  1. Pooled it
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  3. Pooled it
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  7. Immediate postpartum insertion of intrauterine device for contraception.The Cochrane database of systematic reviews · 2015
    Pooled it
  8. Pooled it
  9. Trial
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  13. Immediate Versus Delayed Insertion of the Levonorgestrel Intrauterine Device in Postpartum Adolescents: A Randomized Pilot Study.Hawai'i journal of medicine & public health : a journal of Asia Pacific Medicine & Public Health · 2018
    Trial
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  15. Trial
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  18. Article
  19. U.S. Medical Eligibility Criteria for Contraceptive Use, 2024.MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports · 2024
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 1 country.

Beatrice A ChenDepartment of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA. chenba@upmc.edu
Matthew F Reeves
Jennifer L Hayes
Heather L Hohmann
Lisa K Perriera
Mitchell D Creinin
University Hospitals of Cleveland · USCase Western Reserve University · USContraception Research and Development · USMagee-Womens Research Institute · USWomen's Hospital · US

Funding

UNIVERSITY OF PITTSBURGH CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE: BPCAUL1RR024153 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2006 to 2011
$73.9M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
NCATS NIH HHS UL1 TR000005NCRR NIH HHS 1 UL1 RR024153NCRR NIH HHS UL1 RR024153
6 · The paper itself

Abstract

objectiveTo estimate whether 6-month use of the levonorgestrel-releasing intrauterine device (IUD) would be higher when insertion occurred within 10 minutes of placental delivery compared with 6-8 weeks postpartum.

methodsWe enrolled pregnant women planning vaginal deliveries and desiring a postpartum levonorgestrel-releasing IUD. Patients were randomly assigned when admitted in labor to postplacental or delayed IUD insertion. The women followed up in person at 6-8 weeks and 6 months and were contacted by telephone at 3 months. Women were ineligible for a study IUD postenrollment for intrapartum events including infection, hemorrhage, and cesarean delivery; these women were contacted by phone at 3 and 6 months. Expelled IUDs were replaced per patient preference.

resultsSuccessful IUD placement occurred in 50 of 51 participants (98.0%) and 46 of 51 participants (90.2%) in the postplacental and delayed groups, respectively (P=.2). Expulsion within 6 months occurred in 12 of 50 (24.0%; 95% confidence interval [CI], 13.1-38.2) and two of 46 (4.4%; 95% CI 0.5-14.8) participants, respectively (P=.008). Intrauterine device use at 6 months was 43 of 51 (84.3%; 95% CI 71.4-93.0) and 39 of 51 (76.5%; 95% CI 62.5-87.2), respectively (P=.32). For ineligible patients, only 11 of 41 (26.8%) women were using IUDs at 6 months and two (4.9%) had become pregnant.

conclusionIntrauterine device use 6 months after delivery is similar in women who have postpartum or scheduled delayed IUD placement through a study after replacement of expelled IUDs. Expulsions are significantly higher with postplacental compared with delayed IUD placement. Women asked to follow up with their own health care providers for delayed insertion are significantly less likely to receive an IUD. CLINICAL

trial registrationClinicalTrials.gov, www.clinicaltrials.gov, NCT00476021. LEVEL OF EVIDENCE: I.

Indexed as

Intrauterine Devices, MedicatedPostpartum PeriodAdultContraceptive Agents, FemaleFemaleHumansIntrauterine Device ExpulsionLevonorgestrelPregnancyTime FactorsContraceptive Agents, FemaleLevonorgestrel

Identifiers

PMID20966692
PMCPMC3104850
OpenAlexW2168475211

What OpenQuestion holds

Textmetadata
LicenceTDM
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.