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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05109377
Other study ID # E-93471371-514.10
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 24, 2021
Est. completion date December 15, 2021

Study information

Verified date November 2021
Source Ankara Training and Research Hospital
Contact Veysel Bayburtluoglu
Phone +905530299981
Email bayburtluogluveysel@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators analyze the patients' endocan levels, IIEF scores, and hormon levels both before and after tadalafil (5 or 20mg) treatment. The investigators want to see erectile dysfunction severity and tadalafil treatment relations with endocen level.


Description:

The investigators will include at least 90 patients in study. Blood tests will taken before and after tadalafil treatment and will store at -80 celcius degree.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date December 15, 2021
Est. primary completion date November 15, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: • Patients with erectile dysfuction Exclusion Criteria: - Psychogenic erectile dysfunction - Erectile dysfunction associated with hormonal disorders - Drug related erectile dysfunction

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Endocan
Endocan will measured before and after treatment
Drug:
tadalafil
tadalafil

Locations

Country Name City State
Turkey Veysel Bayburtluoglu Ankara

Sponsors (1)

Lead Sponsor Collaborator
Ankara Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rates of IIEF Score Levels of Endocan relationship with IIEF 1 month
Secondary Levels of Endocan Levels of Endocan with tadalafil treatment 1 month
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