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Effect of Udenafil Administration for Cerebral Blood Flow Increase

Effect of Udenafil Administration for Blood Flow Increase in the Prefrontal Cortex

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0005833
Enrollment
10
Registered
2021-01-27
Start date
2020-12-01
Completion date
Unknown
Last updated
2024-11-14

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

Conditions

None listed

Interventions

Drug : Intervention group 1 takes Udenafil, 100mg once daily, orally for the first 3 days, and then does not take the drug for 3 days. Intervention group 2 does not take the drug for the first 3 days,

Sponsors

Jeonbuk National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: -Adult males aged 55 to 65 years old -After hearing and understanding the detailed explanation of this study, the subject voluntarily decides to participate in the study and gives written consent -When the MMSE score is taken into account of age, gender, and education level, it is at a normal level of mean-1SD or higher. -Those who are willing to cooperate with this study and complete all phases of clinical trials, and who are practically viable

Exclusion criteria

Exclusion criteria: 1. If you have a history of stroke, myocardial infarction, or CABG surgery within the past 6 months 2. Has a history of cardiac failure, unstable angina, or life-threatening arrhythmia within the last 6 months 3. If you have uncontrolled diabetes 4. If you have proliferative diabetic retinopathy 5. Spinal cord injury, radical prostatectomy and radical pelvic surgery 6. If you have hypotension of less than 90/50mmHg or uncontrolled hypertension of more than 170/100mmHg 7. If there is an abnormality in liver function or kidney function 8. If you have retinitis pigmentosa 9. Severe active peptic ulceration within the past year 10. If you have a blood disorder (sickle cellosis, multiple myeloma, leukemia) or bleeding disorder that may predispose to persistent erection 11. In case the researcher determines that it is unsuitable for participation in the test, such as mental disorder or continuous abuse of drugs 12. When taking Nitrates/Nitric oxide(NO) donor (ex. nitroglycerin, isosorbide mononitrate, isosorbide dinitrate, amyl nitrate/nitrite, Sodium nitroprusside) 13. If you are being treated with cancer chemotherapy 14. If you are taking anticoagulants 15. Taking drugs or foods that affect the metabolism of CYP3A4 in the liver 16. If you are taking Androgens (ex. testosterone) or anti-androgens 17. Use of other PDE-5 inhibitors (Viagra®, Levitra® and Cialis®) or other erectile dysfunction treatments for the treatment of erectile dysfunction within 2 weeks prior to trial 18. History of hypersensitivity to other PDE-5 inhibitors (Viagra®, Levitra® and Cialis®)

Design outcomes

Primary

MeasureTime frame
Reactive brain blood flow obtained by near-infrared spectroscopy

Secondary

MeasureTime frame
Cognitive function test result

Countries

Korea, Republic of

Contacts

Public ContactKo Woon Kim

Jeonbuk National University Hospital

kowoonkim@jbnu.ac.kr+82-63-250-1582

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026