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Dietary Supplement
Nitric Oxide Supplement for Prehypertension
Phase 1 & 2
Waitlist Available
Led By Ernst Schwarz, MD, PhD
Research Sponsored by Neogenis Laboratories
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Must not have
Existence of any significant internal or cardiovascular disease
Current use of any antihypertensive medication
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days
Summary
This trial is testing a lozenge called Neo40(TM) that contains nitrates. It aims to help healthy adults who have slightly high blood pressure. The lozenge works by widening blood vessels, which can lower blood pressure. Neo40(TM) lozenge contains nitrates, which have been shown to reduce blood pressure by converting to nitric oxide, a vasodilator.
Who is the study for?
This trial is for adults aged 18-80 with prehypertension, which means their blood pressure readings are at or above 135/80 mmHg. Participants must be able to give informed consent and follow the study's procedures. Those with serious internal or heart diseases, using blood pressure meds, or unable to consent are excluded.
What is being tested?
The study tests if Neo40(TM), a nitric oxide supplement taken orally as a lozenge, can lower blood pressure in prehypertensive adults compared to a placebo (a dummy pill).
What are the potential side effects?
Potential side effects of the nitric oxide supplement may include headaches, dizziness due to low blood pressure, possible stomach upset or changes in heart rate. Placebo effects should have no active side effects but can cause similar symptoms due to psychological factors.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a serious heart or internal disease.
Select...
I am currently taking medication for high blood pressure.
Select...
I am able to give informed consent and follow up on my treatment.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Reduction in Systolic and Diastolic Blood Pressure Readings
Secondary study objectives
Improvement in Functional Capacity
Other study objectives
Improvement in Quality of Life
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: Nitric Oxide supplementActive Control1 Intervention
Group II: PlaceboPlacebo Group1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for hypertension often focus on vasodilation to reduce blood pressure. Nitrate-based treatments, like Neo40(TM), work by increasing nitric oxide (NO) production, which relaxes blood vessels and improves blood flow.
This mechanism is crucial for hypertension patients as it directly reduces vascular resistance and lowers blood pressure. Other common treatments include ACE inhibitors and ARBs, which block the effects of angiotensin II, a molecule that constricts blood vessels, and calcium channel blockers, which relax blood vessel muscles.
These treatments are essential for managing hypertension and preventing complications such as stroke and heart disease.
Antihypertensive treatment and endothelium-dependent venodilation in sleep-disordered breathing.Nitric oxide and atherosclerotic lesion progression: an overview.[The activation of soluble guanylate cyclase by new NO donors as the basis of a directed search for new efficacious vasodilators and antiaggregants].
Antihypertensive treatment and endothelium-dependent venodilation in sleep-disordered breathing.Nitric oxide and atherosclerotic lesion progression: an overview.[The activation of soluble guanylate cyclase by new NO donors as the basis of a directed search for new efficacious vasodilators and antiaggregants].
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Neogenis LaboratoriesLead Sponsor
5 Previous Clinical Trials
164 Total Patients Enrolled
2 Trials studying Hypertension
109 Patients Enrolled for Hypertension
Ernst Schwarz, MD, PhDPrincipal InvestigatorCalifornia Medical Institute, Cedars Sinai Medical Center
1 Previous Clinical Trials
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Your blood pressure is consistently at or above 135/80 mmHg when you are resting.I have a serious heart or internal disease.I am currently taking medication for high blood pressure.I am able to give informed consent and follow up on my treatment.I am between 18 and 80 years old.
Research Study Groups:
This trial has the following groups:- Group 1: Placebo
- Group 2: Nitric Oxide supplement
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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