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Effects of Tadalafil on LMR and MHR in Patients With ED

Evaluation of the Effects of a Daily Dose of 5 mg of Tadalafil on Lymphocyte to Monocyte Ratio and Monocyte to High-Density Lipoprotein Ratio in Patients With Erectile Dysfunction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03918993
Enrollment
62
Registered
2019-04-18
Start date
2019-02-14
Completion date
2019-04-05
Last updated
2019-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erectile Dysfunction, Inflammation

Keywords

Erectile Dysfunction, lymphocyte to monocyte ratio, monocyte to HDL ratio

Brief summary

The aim of the study was to investigate whether daily 5 mg tadalafil over eight weeks affects to Lymphocyte/Monocyte ratio (LMR) and Monocyte/High-Density Lipoprotein ratio (MHR) in patients with erectile dysfunction (ED). Thirty-one patients with organic ED and 31 healthy controls between July 2017 and November 2018 were included in this retrospective study. To avoid bias, the patients were randomly selected and the controls were also incorporated consecutively. The presence of ED was determined according to the International Erectile Function Index-5 (IIEF-5). The patients and the controls were evaluated in terms of IIEF-5, complete blood count, serum biochemistry, LMR, and MHR.

Detailed description

The medical records of the heterosexual men treated with the diagnosis of organic ED in the Urology department of a private hospital between July 2017 and October 2018 were evaluated retrospectively. The number of samples to be included in the study was determined by the help of the computer-assisted power analysis. Random sampling was performed from all cohorts of patients with ED. Thirty-one male patients between the ages of 39-65 with organic erectile dysfunction more than one year and treated with OAD 5 mg dose of tadalafil for eight weeks were selected as the treatment group (group T)The patients in group T have been assessed both before (T1) and after (T2) the treatment. Between the ages of 39-65, thirty-one healthy men who were admitted to the internal medicine outpatient clinic for their annual follow-up were selected consecutively and the control group (group C) was formed. All subjects in the control group were sexually active men with regular monogamous heterosexual relationships during the last one year. .

Interventions

DRUGTadalafil 5mg tablet

Once-a-day 5 mg dose of tadalafil for 8 weeks

Sponsors

Ondokuz Mayıs University
CollaboratorOTHER
Samsun Liv Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
39 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* 39-65 years old men with ED * 39-65 years old, haelthy men * Patients that have received 5 mg tadalafil/day for 8 weeks * Patients with informed consent forms * Patients with no missing variables

Exclusion criteria

* Patients with systemic autoimmune and inflammatory disease, * congestive heart failure, * chronic renal failure, and chronic hepatobiliary disease, * chronic lung disease, and thyroid dysfunction, * patients with acute infection, * patients with neurological deficits, * metabolic syndrome and malignancy * Patients with a history of prostate, penile or pelvic surgery or radiotherapy,, * patients receiving anticoagulant, beta-blocker, antidepressants and antipsychotics, hormonal therapy, * patients with alcohol and smoking

Design outcomes

Primary

MeasureTime frameDescription
Lymphocyte to Monocyte Ratioup to 8 weeksratio of values in complete blood count
monocyte to HDL ratioup to 8 weeksan inflamamtoy marker
The International Index of Erectile Function (IIEF-5) Questionnaireup to 8 weeksIIEF-5 scoring: The IIEF-5 score is the sum of the ordinal responses to the 5 items. 22-25: No erectile dysfunction 17-21: Mild erectile dysfunction 12-16: Mild to moderate erectile dysfunction 8-11: Moderate erectile dysfunction 5-7: Severe erectile dysfunctio
monocyte countup to 8 weekscomplete blood count
lymphocyte countup to 8 weekscomplete blood count
HDL cholesterolup to 8 weeksserum lipid profile
Testosteronup to 8 weekshormonal evaluation
fasting glucoseat the 1st dayserum glucose level

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026