Health Condition 1: N529- Male erectile dysfunction, unspecified
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Male subjects between the ages of 20 to 60 years. 2. Patients willing to participate and give informed consent. 3. Patients not having many complications or many secondary infections. 3. Participants with serum testosterone levels between 280 and 350 ng per dl Established diagnosis of erectile dysfunction (ED) for over 6 months and less than 5 years, had a baseline IIEF EF score between 11 and 25. 4. Those who were in a stable relationship for over 5. months with a minimum of 2 sexual attempts per month for at least 1 month prior to enrollment.
Exclusion criteria
Exclusion criteria: 1. Hypogonadism or anatomical deformity of the penis such as severe penile fibrosis. 2. History of significant pathological cardiovascular conditions such as congestive heart failure, lifethreatening arrhythmia or ischemic heart disease 3. Continuing history of alcohol and or drug abuse. 4. Subjects with neuromuscular disorders. 5. Subjects with secondary hypertension 6. Cases with severe diabetic complications such as cardiac disease, nephropathy, and foot ulcer. 7. Participation in other clinical trials. 8. Unwilling or unable to sign the informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To evaluate increase in blood flow, blood flow retention and visible veins on organ. 2. To evaluate blockage revival. 3. To evaluate the increase in Testosterone levels.Timepoint: Day 1, Day 10, Day 20, Day 30 | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To investigate the general immune functions 2. To evaluate changes in energy levels and libido. 3. To evaluate improvement in mood and stress levels.Timepoint: Day 1, Day 10, Day 20, Day 30 | — |
Countries
India
Contacts
Samahitha Research Solutions