Evidence map›Paper›PMID 42558224›Full record

Trial reportFrontiers in endocrinology2026

An automatic semen processing system versus a manual method for semen processing: a randomized, single-blind non-inferiority trial.

Qiuxia Yan, Chen Zeng, Guozhi Zhang, Jing Qiao, Huyu Zhou, Zhenjie Zhu, Ling Feng, Xiaoying Zhao, Hong Hu, Piaoyan Zhou and 5 more

Abstract readComparative StudyEquivalence TrialRandomized Controlled Trial
In one paragraph

Trial report in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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.

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

15 authors.

Qiuxia YanCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Chen ZengCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Guozhi ZhangCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Jing QiaoCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Huyu ZhouDepartment of Obstetrics and Gynecology, Center for Reproductive Medicine, Guangdong Provincial Key Laboratory of Major Obstetric Diseases, Guangdong Provincial Clinical Research Center for Obstetrics and Gynecology, Guangdong-Hong Kong-Macao Greater Bay Area Higher Education Joint Laboratory of Maternal-Fetal Medicine, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Zhenjie ZhuCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Ling FengCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Xiaoying ZhaoCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Hong HuCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Piaoyan ZhouCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Wanting HuangCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Xiuqin ZhouCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Lei LiDepartment of Obstetrics and Gynecology, Center for Reproductive Medicine, Guangdong Provincial Key Laboratory of Major Obstetric Diseases, Guangdong Provincial Clinical Research Center for Obstetrics and Gynecology, Guangdong-Hong Kong-Macao Greater Bay Area Higher Education Joint Laboratory of Maternal-Fetal Medicine, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Cairong ChenCenter for Reproductive Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Guangdong Engineering Technology Research Center of Urinary Continence and Reproductive Medicine, Qingyuan, China.
Jianqiao LiuDepartment of Obstetrics and Gynecology, Center for Reproductive Medicine, Guangdong Provincial Key Laboratory of Major Obstetric Diseases, Guangdong Provincial Clinical Research Center for Obstetrics and Gynecology, Guangdong-Hong Kong-Macao Greater Bay Area Higher Education Joint Laboratory of Maternal-Fetal Medicine, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In assisted reproductive technology (ART) laboratories, semen processing is traditionally performed using manual density gradient centrifugation (DGC), which is labor intensive, time consuming, and subject to inter-technician variability. This study aimed to evaluate the effectiveness and repeatability of an automatic semen processing system (Avensen (Shenzhen) Medical Tech Co., Ltd., Shenzhen, China) compared with the standard manual method. Methods: A total of 110 eligible male participants (aged 18-45 years) were enrolled. Each semen sample was randomized into three 1-mL aliquots, of which two were processed automatically (automated groups 1 and 2) and one manually (manual group). Independent t-tests were used to compare the progressively motile sperm recovery rate between the automated and manual groups. System repeatability was assessed between the two automated groups using the intraclass correlation coefficient, the coefficient of variation, and Bland-Altman analysis. Results: The automatic system was non-inferior to the manual method in terms of the primary outcome. The progressively motile sperm recovery rate were 42.26% and 42.40% in automated groups 1 and 2, respectively, versus 41.64% in the manual group. The lower 95% confidence limits were -1.39% and -1.37%, both exceeding the -6% non-inferiority margin. Post-processing percentage of progressively motile sperm (PR%) was significantly higher in both automated groups: 62.06% and 62.63% versus 58.83% (P<0.001). No significant differences were found in sperm concentration or total motile count (P>0.05). Repeatability was excellent: the recovery rate had an intraclass correlation coefficient of 0.95 (95% CI: 0.93-0.97) and a mean coefficient of variation of 10.87%. Correlation analysis (r=0.9092), Deming regression (slope=1.0277), and Bland-Altman analysis (mean difference -0.1448%, 95.41% within limits) indicated strong agreement without bias. Conclusion: The investigated automatic semen processing system is non-inferior to the standard manual method in terms of the progressively motile sperm recovery rate, and the results show high repeatability and consistency. The automatic semen processing system can help technicians reduce their workload, improve work efficiency, and better meet clinical needs. Clinical trial registration: https://www.chictr.org.cn/showproj.html?proj=274183, identifier ChiCTR2500105131.

Indexed as

SemenSemen AnalysisSemen PreservationAdolescentAdultAutomationHumansMaleMiddle AgedReproducibility of ResultsSingle-Blind MethodSperm MotilityYoung Adultautomatic semen processing systemmanual methodnon-inferiorityprogressively motile sperm recovery ratesemen processing

Identifiers

PMID42558224
PMCPMC13437289

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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.