The Effects of a Nitrate Supplementation on Erectile Function

Phase

N/A

Condition

Erectile Dysfunction

Infertility

Impotence

Treatment

Nitric Oxide

Placebo

Tadalafil

Clinical Study ID

NCT06213077

#EDSupp23

Ages 40-65
Male
Accepts Healthy Volunteers

Study Summary

Twenty (20) individuals to be recruited from Ballantyne Medical Associates in Charlotte, NC, without any significant chronic medical history. These patients are general patients for primary care that meet inclusion criteria. Patients will be screened and enrolled by Dr. Bauer and his delegated research staff upon patient consult. Patients will be informed of the purpose of the study including risks, benefits, and alternative treatments to the study. After the potential participants have been given the opportunity to ask questions and have their questions answered, they will be asked to sign an informed consent prior to any study-specific procedures being performed.

Blinded test product will be randomly assigned to study subjects. Test group 1 will be dosed with a placebo capsule taken two capsules once daily Test group 2 will be dosed with Berkeley Life capsules taken two capsules once daily. At baseline, prior to crossover to the other treatment, and at the study's conclusion, NO levels will be monitored using salivary nitric oxide test strips. Both test groups will remain on their existing treatment protocol throughout the study.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Subjects Male between the ages of 40 and 65
Subjects looking to support healthy sexual function who have been undergoing treatmentto support healthy erections for at least 90 days with unsatisfactory results andwhose nitric oxide levels are suboptimal based on an easy-to-use, self-check salivastrip that provides immediate, real-time, actionable feedback.
Patients who are able to sign informed consent.

Exclusion

Exclusion Criteria:

Patients who are not considered medically stable (history of drug or alcoholdependency or having experienced health issues which could prevent experiencing ahealthy erection).
Patients with any known allergy to ingredients of capsule.
Patients currently taking organic nitrates for acute angina
Patients who do not or cannot tolerate PDE5 inhibitors
Patients are unwilling or unable to provide informed consent.

Study Design

Nitric Oxide

December 12, 2023

May 30, 2024

Study Description

Patients will be consented and enrolled in the study. A complete medical history and focused physical examination will be conducted and documented and NO levels will be measured using salivary test strips.

Twenty (20) patients with low NO levels will be enrolled and will be randomly assigned to group 1 or group 2.

Once enrolled, patients will be required to complete a subjective questionnaire (the International Index of Erectile Function (IIEF)), EHS Score questionnaire and a Quality of Life (QOL) survey. Patients will be instructed to take 2 Berkeley Life capsules once daily or the placebo based on randomization. The (IIEF) was developed by Rosen and colleagues in 1997 as a multidimensional, 15-item, self-administered questionnaire with the goal of assessing five domains of male sexual function including erectile function, orgasmic function, sexual desire, intercourse satisfaction, and overall satisfaction. The erectile function domain of the IIEF (IIEF-EF) contains 6 questions which the patient answers on a scale from 1 (never or almost never) to 5 (almost always or always), providing a total score of 6 to 30 points. The questions concern erectile frequency, firmness, penetration ability, maintenance frequency, maintenance ability, and erection confidence. Based on a controlled study of 1,151 men taking sildenafil in order to establish cutoff scores for the IIEF-EF, a score of 26 or greater is defined as normal function, mild ED is a score from 22 to 25, mild to moderate ED 17 to 21, moderate ED 11 to 16, and severe ED 6 to 10.

Patients will be sent home with instructions to take 2 Berkeley Life capsules once daily in combination with their existing treatment protocol and then return on day 60, returning all unused test product.

The subject should be willing to self-administer 2 capsules daily and be willing to, upon waking in the AM, self-test with strip and record on a pre-print sheet the test strip color, followed by self-administration of capsule(s) and then at 2 hours self-test again and record on a pre-print sheet the test strip color.

Upon the return visit, patients will be crossed over after a 4 week wash out and given the other test group combination.

After 60 days of each combination, placebo and active, patients will repeat the IIEF questionnaire, EHS Score questionnaire and the Quality of Life survey.

The remaining product will be collected, and patients released from the study. Data will be collected on Case Report Forms.

Connect with a study center

OnSite Clinical Solutions
Charlotte, North Carolina 28277
United States
Active - Recruiting

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