Evidence map›Paper›PMID 31217822›Full record

ArticleTherapeutic advances in urology

Efficacy and tolerability of

Raúl Guzmán, Julio C Fernández, Manuel Pedroso, Lilia Fernández, José Illnait, Sarahí Mendoza, Ana T Quiala, Zunilda Rodríguez, Jilma Mena, Aylim Rodíguez and 4 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in urology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

14 authors at 1 institution in 1 country.

Raúl GuzmánSalvador Allende Hospital, Havana, Cuba.
Julio C FernándezNational Center for Scientific Research, 25 Avenue and 158 st, Cubanacan, Playa, Havana, 113000, Cuba.ORCID https://orcid.org/0000-0001-8144-4129
Manuel PedrosoSalvador Allende Hospital, Havana, Cuba.
Lilia FernándezNational Center for Scientific Research, Havana, Cuba.
José IllnaitNational Center for Scientific Research, Havana, Cuba.
Sarahí MendozaNational Center for Scientific Research, Havana, Cuba.
Ana T QuialaSalvador Allende Hospital, Havana, Cuba.
Zunilda RodríguezSalvador Allende Hospital, Havana, Cuba.
Jilma MenaSalvador Allende Hospital, Havana, Cuba.
Aylim RodíguezMedical Surgical Research Center, Havana, Cuba.
Marbelis CamposMedical Surgical Research Center, Havana, Cuba.
Carlos SánchezNational Clinical Trials Coordinator Center, Havana, Cuba.
Yanet AlvarezNational Clinical Trials Coordinator Center, Havana, Cuba.
Gladys JiménezNational Clinical Trials Coordinator Center, Havana, Cuba.
Cuban Neuroscience Center · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBenign prostatic hyperplasia (BPH), a common urological disease in aging men, frequently produces lower urinary tract symptoms (LUTS). Clinical studies have shown that terazosin relaxes the smooth muscle of the prostate and bladder, facilitates bladder emptying, improves LUTS, increases maximum urinary flow, and reduces the residual volume of urine. D-004, a lipid extract of the fruit of the Cuban royal palm (

methodsThe present phase III study had an open, randomized, comparative design, with two parallel groups who received D-004 (320 mg/day) or terazosin (5 mg/day) for 6 months. The study included men at least 50 years of age, with evidence of the LUTS of moderate intensity according to the International Symptoms of the Prostate (IPSS). The effects on the IPSS Scale was the primary efficacy variable. The effects on the size of the prostate and the residual volume were secondary variables. The subjective self-perception of symptom relief at trial completion was a collateral outcome. Analysis was done by intention-to-treat.

resultsThe study included 100 men with a diagnosis of BPH, confirmed by digital rectal examination and ultrasonography, and moderate LUTS (IPSS score >7, <19). Baseline characteristics were similar in both groups. Nine patients did not continue the study: one from group D-004 (due to protocol violation) and eight from the terazosin group (six due to adverse events and two due to protocol violation;

conclusionsD-004 administered at a dose of 320 mg/day for 6 months showed comparable efficacy with terazosin (5 mg/day) in reducing the LUTS (IPSS score), producing a significant decrease in prostate volume and postvoid residual volume. Both treatments were safe, with better tolerability for D-004 as compared with terazosin.

Indexed as

benign prostate hyperplasiaD-004IPSSLUTSterazosin

Identifiers

PMID31217822
PMCPMC6560798
OpenAlexW2949748718

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.