Evidence map›Paper›PMID 29667763›Full record

Trial reportThe Journal of dermatology2018

Prospective randomized study of sexual function in men taking dutasteride for the treatment of androgenetic alopecia.

Tsen-Fang Tsai, Gwang Seong Choi, Beom Joon Kim, Moon-Bum Kim, Chi Fai Ng, Puja Kochhar, Stacy Jasper, Betsy Brotherton, Barbara Orban, Zrinka Lulic

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of dermatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Post-finasteride syndrome.Anais brasileiros de dermatologia
    Article
  7. Article
  8. 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

10 authors at 8 institutions in 5 countries.

Tsen-Fang TsaiNational Taiwan University Hospital, Taipei, Taiwan.
Gwang Seong ChoiInha University Hospital, Incheon, South Korea.
Beom Joon KimChung-Ang University Hospital, Seoul, South Korea.
Moon-Bum KimPusan National University Hospital, Busan, South Korea.ORCID http://orcid.org/0000-0003-1616-1784
Chi Fai NgSH Ho Urology Center, The Chinese University of Hong Kong, Hong Kong, China.
Puja KochharGSK, Mumbai, India.ORCID http://orcid.org/0000-0001-9931-1658
Stacy JasperGSK, Research Triangle Park, North Carolina, USA.
Betsy BrothertonPAREXEL International, Durham, North Carolina, USA.
Barbara OrbanGSK, Research Triangle Park, North Carolina, USA.
Zrinka LulicGSK, Brentford, Middlesex, UK.
Research Triangle Park Foundation · USChinese University of Hong Kong · HKChung-Ang University Hospital · KRGlaxoSmithKline (India) · INInha University Hospital · KRNational Taiwan University Hospital · TWPAREXEL International (United States) · USPusan National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment with 5α-reductase inhibitors has been associated with sexual adverse events such as impotence (erectile dysfunction) and decreased libido. The primary objective of this study was to evaluate adverse events related to sexual function, based on their frequency, duration, persistence and associated treatment discontinuations, in men treated with dutasteride for androgenetic alopecia. Participants were randomized to receive double-blind dutasteride 0.5 mg or placebo once daily for 24 weeks, followed by open-label dutasteride 0.5 mg for an additional 24 weeks. Sexual adverse events were followed up until resolution or for up to 24 weeks after the last dose. Overall, 117 men, 23-50 years of age, were randomized. The incidence of sexual adverse events was approximately twofold higher in the dutasteride group (16%) than the placebo group (8%) during the double-blind period; the overall incidence of sexual adverse events was lower (5%) during the open-label period. All adverse events were mild to moderate in severity and considered treatment-related. The adverse events resolved while on study treatment or after the end of treatment and did not lead to treatment discontinuation. A limitation of this study was the small sample size. The sexual adverse events of impotence, decreased libido and ejaculation disorders reported in this study were expected and reversible.

Indexed as

5-alpha Reductase InhibitorsAdultAge FactorsAlopeciaDouble-Blind MethodDutasterideHumansIncidenceLibidoMaleMiddle AgedPlacebosProspective StudiesSexual Dysfunctions, PsychologicalTreatment OutcomeYoung Adult5-alpha Reductase InhibitorsDutasteridePlacebosandrogenetic alopeciadutasterideerectile dysfunctionlibidosexual function

Identifiers

PMID29667763
PMCPMC6055634
OpenAlexW2802078918

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.