Evidence map›Paper›PMID 42295466›Full record

Observational studyArchives of gynecology and obstetrics2026

Safety and effectiveness of etonogestrel implant in Chinese women requiring contraception: a multicenter, prospective, observational study.

Xinyan Liu, Xiaoye Wang, Xiao'ou Xu, Yanfei Zhou, Wenxia Ma, Li Jiang, Qiwei Qi, Jian Li, Tinghui Yu, John W Grunden and 1 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Archives of gynecology and obstetrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Xinyan Liu *National Clinical Research Center for Women's Health and Obstetric and Gynecologic Diseases, Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Peking, China.
Xiaoye Wang *National Clinical Research Center for Obstetrics and Gynecology, Department of Obstetrics and Gynecology, Peking University Third Hospital, Peking, China.
Xiao'ou XuChongqing Population and Family Planning Science and Technology Research Institute, Chongqing, China.
Yanfei ZhouDepartment of Gynecology, Changsha Maternal and Child Health Hospital Affiliated to Hunan Normal University, Changsha, Hunan, China.
Wenxia MaHenan Academy of Innovations in Medical Science, Zhengzhou, Henan, China.
Li JiangDepartment of Gynecology, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi, China.
Qiwei QiQingdao Women and Children's Hospital, Qingdao University, Qingdao, Shandong, China.
Jian LiMedical Affairs and Outcome Research, Organon China, Shanghai, China.
Tinghui YuOrganon Co., New Jersey, USA.
John W GrundenMedical Affairs and Outcome Research, Organon Co., New Jersey, USA.
Chengliang XiongInstitute of Reproductive Health/Center of Reproductive Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. clxiong951@sina.com.ORCID http://orcid.org/0000-0002-2321-1009

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess the overall safety and effectiveness of the etonogestrel implant radiopaque in real-world clinical settings in China.

methodsA multicenter, prospective, single-arm, observational study was conducted in women (aged ≥ 18 years) across 31 centers in China (March 2016-July 2021). The implant was prescribed as part of routine clinical practice. Primary outcomes included overall safety and topical (local) safety profile; secondary outcomes included participant and physician satisfaction and contraceptive effectiveness of the etonogestrel implant.

resultsOf 1,901 women using the etonogestrel implant, 45.5% completed the 3-year study. The mean (SD) age of the women was 32.1 (5.6) years and the mean (SD) implant exposure duration was 783.7 (388.7) days. Overall, 47.9% reported drug-related adverse events (AEs; excluding topical AEs), 1.1% reported serious AEs, and 10.4% reported topical AEs after insertion. Vaginal bleeding (15.6%) was the most frequent drug-related AE. At 36 months after insertion or upon removal, most women were satisfied (38.9%) or very satisfied (23.7%) with the implant. Among 96 physicians who completed questionnaires following the first insertion, 57.3% were very satisfied and 38.5% were satisfied. Most (98.9%) of the physicians reported satisfaction following their first removal procedure. Of them, 65.3% were very satisfied and 33.7% were satisfied. One (1.1%) physician was neither satisfied nor dissatisfied. One (0.05%) in-treatment pregnancy was reported.

conclusionSafety findings from this study in China's real-world clinical setting were consistent with the clinical development program without unexpected safety signals. Observed contraceptive effectiveness was consistent with established evidence for the implant, with general satisfaction reported among Chinese women.

Indexed as

Contraceptive Agents, FemaleDesogestrelAdultChinaContraceptive EffectivenessDrug ImplantsEast Asian PeopleFemaleHumansPatient SatisfactionPregnancyProspective StudiesUterine HemorrhageYoung AdultContraceptive Agents, FemaleDesogestrelDrug ImplantsetonogestrelContraceptive implantEffectivenessEtonogestrelSafetySatisfaction

Identifiers

PMID42295466
PMCPMC13503388

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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.