Evidence map›Paper›PMID 33529810›Full record

ArticleSexual medicine2021

Safety and Effectiveness of Dapoxetine On Demand in Chinese Men With Premature Ejaculation: Results of a Multicenter, Prospective, Open-Label Phase IV Study.

Jing Peng, Lin Yang, Long Liu, Renyuan Zhou, Jihong Liu, Ningchen Li, Liming Li, Yongguang Jiang, Yuqiang Liu, Zhaohui Zhu and 5 more

Open access · goldAbstract read
In one paragraph

Article in Sexual medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 46% 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.

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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. Review
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 at 11 institutions in 2 countries.

Jing PengAndrology Center, Department of Urology, Peking University First Hospital, Peking University, Beijing, China.
Lin YangDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Long LiuDepartment of Urology, North Theater General Hospital, Shenyang, China.
Renyuan ZhouDepartment of Urology, Shanghai Jingan District Central Hospital, Shanghai, China.
Jihong LiuDepartment of Urology, Tongji Hospital Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Ningchen LiDepartment of Urology, Peking University Shougang Hospital, Beijing, China.
Liming LiDepartment of Urology, General Hospital of Tianjin Medical University, Tianjin, China.
Yongguang JiangDepartment of Urology, Beijing Anzhen Hospital of Capital Medical University, Beijing, China.
Yuqiang LiuDepartment of Urology, Second Hospital of Shandong University, Ji'nan, China.
Zhaohui ZhuDepartment of Urology, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Xiaodong ZhangDepartment of Urology, Beijing Chaoyang Hospital of Capital Medical University, Beijing, China.
Guowei ShiDepartment of Urology, Shanghai Fifth People's Hospital of Fudan University, Shanghai, China.
Suyog JainMedical Department, A Menarini Asia Pacific, Singapore.
Emmanuele A JanniniChair of Endocrinology and Medical Sexology (ENDOSEX), Department of Systems Medicine, University of Rome Tor Vergata, Rome, Italy.
Zhichao ZhangAndrology Center, Department of Urology, Peking University First Hospital, Peking University, Beijing, China. Electronic address: zhangzhichao@bjmu.edu.cn.
Capital Medical University · CNPeking University · CNFirst Affiliated Hospital of Xi'an Jiaotong University · CNFudan University · CNJingzhou Central Hospital · CNPeking University Shougang Hospital · CNSecond Hospital of Shandong University · CNTianjin Medical University General Hospital · CNTongji Hospital · CNUnion Hospital · CNUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDapoxetine on demand has been approved for premature ejaculation (PE) management in China; however, studies on the efficacy and safety of this treatment in the Chinese population are scarce.

aimThe aim of this study was to evaluate the safety and effectiveness of dapoxetine 30 mg and 60 mg on demand in Chinese men with PE.

methodsPhase IV real-world study on 1,252 patients with PE. If men reported no response to dapoxetine 30 mg after 4 weeks treatment, dapoxetine has been uptitrated at 60 mg for 4 weeks more.

main outcome measureSelf-reported data were collected for demographics, general and sexual health characteristics, PE severity, and treatment safety and effectiveness, as measured by the PE profile questionnaire.

resultsAdverse events (AEs), such as nausea, thirst, headache, and dizziness, similarly to previous literature, were detected. The treatment-emergent AEs rate was higher in the patients treated with 30 and 60 mg (n = 192) compared with those treated with the dapoxetine 30 mg only (n = 1060) (34.4% vs 15.8%, respectively). No new safety concerns were observed. The overall effectiveness rates were 88.2% in subjects using 30 mg of dapoxetine, whereas a rescue from the previous failure was in 55.7% in the patients who received 60 mg after the initial 30 mg. Overall, 83.2% responded to dapoxetine at dosages equal to or lower than 60 mg.

conclusionThe results in this study demonstrated in a large Chinese population that on-demand dapoxetine is a safe and effective symptomatic treatment in patients with PE. J Peng, L Yang, L Liu, et al. Safety and Effectiveness of Dapoxetine On Demand in Chinese Men With Premature Ejaculation: Results of a Multicenter, Prospective, Open-Label Phase IV Study. Sex Med 2021;9:100296.

Indexed as

DapoxetineEffectivenessPremature ejaculationSafetySexual dysfunctionTreatment

Identifiers

PMID33529810
PMCPMC8072166
OpenAlexW3128189233

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.