Evidence map›Paper›PMID 35791295›Full record

ArticleThe world journal of men's health2023

Comparison of Intratesticular Testosterone between Men Receiving Nasal, Intramuscular, and Subcutaneous Pellet Testosterone Therapy: Evaluation of Data from Two Single-Center Randomized Clinical Trials.

Parris Diaz, Rohit Reddy, Ruben Blachman-Braun, Isaac Zucker, Alexandra Dullea, Daniel C Gonzalez, Eliyahu Kresch, Ranjith Ramasamy

Open access · diamondAbstract read
In one paragraph

Article in The world journal of men's health, 2023. 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
1.0field-weighted citation impact, top 23% 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

0 citing papers in PubMed, 7 citations in OpenAlex.

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

8 authors at 1 institution in 1 country.

Parris Diaz *Department of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID https://orcid.org/0000-0003-4666-303X
Rohit Reddy *Department of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID https://orcid.org/0000-0003-1032-6656
Ruben Blachman-BraunDepartment of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID https://orcid.org/0000-0001-9700-0805
Isaac ZuckerDepartment of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID https://orcid.org/0000-0001-9051-5400
Alexandra DulleaDepartment of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID https://orcid.org/0000-0003-2213-482X
Daniel C GonzalezDepartment of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID https://orcid.org/0000-0002-2676-1452
Eliyahu KreschDepartment of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID https://orcid.org/0000-0001-8319-0820
Ranjith RamasamyDepartment of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA. Ramasamy@miami.edu.ORCID https://orcid.org/0000-0003-1387-7904
University of Miami · US

Funding

Acerus PharmaceuticalsEmpower Pharmacy
6 · The paper itself

Abstract

purposeTestosterone replacement therapy (TRT) can potentially cause decreased spermatogenesis and subsequent infertility. Recent studies have suggested that 17-hydroxyprogesterone (17-OHP) is a reliable surrogate for intratesticular testosterone (ITT) that is essential for spermatogenesis. We evaluated data from two ongoing open-label, randomized, two-arm clinical trials amongst different treatment preparations (Trial I) subcutaneous testosterone pellets (TP) and (Trial II) intranasal testosterone (NT) or intramuscular testosterone cypionate (TC). MATERIALS AND

methodsSeventy-five symptomatic hypogonadal men (2 serum testosterone <300 ng/dL) were randomized into open label randomized clinical trials. Eligible subjects received 800 mg TP, 11 mg TID NT or 200 mg ×2 weeks TC. 17-OHP and Serum testosterone were evaluated at baseline and follow-up. The primary outcome was changes in 17-OHP. Secondary outcome was changes in serum testosterone. Data was analyzed by two-sample and single-sample t-tests, and determination of equal or unequal variances was computed using F-tests.

resultsMedian participant age was 45 years old, with overall baseline 17-OHP of 46 and serum testosterone of 223.5 ng/dL. 17-OHP significantly decreased in subjects prescribed long-acting TP or TC. The 4-month change in 17-OHP in the NT group (-33.3% from baseline) was less than the change seen in TC (-65.3% from baseline) or TP (-44% from baseline) (p=0.005). All testosterone formulations increased serum testosterone levels at follow-up, with the largest increase seen in TC (+157.6%), followed by NT (+114.3%) and TP (+79.6%) (p=0.005).

conclusionsShort-acting nasal testosterone appear to have no impact on serum 17-OHP especially in comparison to long-acting testosterone formulations. All modalities saw significant increases in serum testosterone levels at follow-up. NT and other short acting testosterone formulations may better preserve ITT and be beneficial for hypogonadal men seeking to maintain fertility potential while on TRT.

Indexed as

17-alpha-HydroxyprogesteroneAndrogensFertilityHypogonadismTestosterone

Identifiers

PMID35791295
PMCPMC10042650
OpenAlexW4226460535

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.