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Testosterone Therapy in Type 2 Diabetes Mellitus Patients with Erectile Dysfunctio

Phase 2
Conditions
Erectile dysfunction.
Male erectile disorder
F52.21
Registration Number
IRCT20181106041575N1
Lead Sponsor
Research and technology deputy of Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
66
Inclusion Criteria

Presence of Erectile dysfunction
Presence of Type 2 Diabetes Mellitus
Normal Serum Testosterone level
IIEF=<16

Exclusion Criteria

Contraindication for Tadalafil consumption including: Heart disease, Hypertension and Nitrocontin consumption
Contraindication for Tadalafil consumption including: liver disorder and prostate cancer

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Erectile dysfunction according to The International Index of Erectile Function (IIEF-5). Timepoint: International Index of Erectile Function (IIEF-5) was completed before, 3-month, and 6-month after the intervention. Method of measurement: erectile dysfunction according to The International Index of Erectile Function (IIEF-5).
Secondary Outcome Measures
NameTimeMethod
The side-effects of the intervention. Timepoint: before and 3-month after the intervention. Method of measurement: the side-effects of the intervention was measured using laboratory findings including liver function test, complete blood count (CBC), liver function test (LFT), fasting blood sugar and Prostate-specific antigen (PSA).
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