Durable BLOOD PRESSURE

Clinical evidence summary

Durable BLOOD PRESSURE®

Durable
BLOOD PRESSURE®

Durable BLOOD PRESSURE was formulated by Dr. Kevin Passero based on 20 years of clinical practice—combining two patented, clinically validated extracts that work through complementary pathways to address the real drivers of high blood pressure.

Every ingredient is backed by peer-reviewed human clinical trials—selected not just for scientific validation, but for results that hold up in the real world.

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Key clinical outcomes 

What the research shows

↓ Systolic BP · Enovita®

−37 pts

Average systolic blood pressure reduction from baseline at 300mg daily over 16 weeks, combined with diet and lifestyle changes, in pre/mildly hypertensive adults.

Belcaro et al. 2013 · PMC3792515 ·
119 adults

↓ Diastolic BP · Enovita®

−9 pts

Average diastolic blood pressure reduction from baseline at 300mg daily over 16 weeks, combined with diet and lifestyle changes, in pre/mildly hypertensive adults.

Belcaro et al. 2013 · PMC3792515 ·
119 adults

↑ Nitric oxide · Enovita® (in vitro)

+154%

eNOS nitric oxide enzyme activation in endothelial cell model—explains vessel-relaxing mechanism.


Petrangolini et al. 2021 · PMC7922661 ·
HUVEC cell study

↓ Endothelin-1 · Enovita® (in vitro)

>80%

Endothelin-1—the peptide that constricts arteries—reduced to near-undetectable levels.

Petrangolini et al. 2021 · PMC7922661 ·
endothelial cell model

↓ Systolic BP · Benolea®

−11 pts

Reduction from baseline at 1,000mg daily over 8 weeks in borderline hypertensive identical twins. 

Perrinjaquet-Moccetti et al. 2008 ·
monozygotic twin RCT · 8 weeks

↓ Systolic BP · Benolea®

−11.5 pts

Systolic BP reduction in 8-week double-blind active-controlled study in 232 stage-1 hypertensive patients.

Susalit et al. 2011 · Phytomedicine ·
232 patients · 8 weeks

↓ Systolic BP · Enovita®

−37 pts

Average systolic blood pressure reduction from baseline at 300mg daily over 16 weeks, combined with diet and lifestyle changes, in pre/mildly hypertensive adults.

Belcaro et al. 2013 · PMC3792515 · 119 adults

↓ Diastolic BP · Enovita®

−9 pts

Average diastolic blood pressure reduction from baseline at 300mg daily over 16 weeks, combined with diet and lifestyle changes, in pre/mildly hypertensive adults.

Belcaro et al. 2013 · PMC3792515 · compliance >94%

↑ Nitric oxide · Enovita® (in vitro)

+154%

eNOS nitric oxide enzyme activation in endothelial cell model—explains vessel-relaxing mechanism.

Petrangolini et al. 2021 · PMC7922661 · HUVEC cell study

↓ Endothelin-1 · Enovita® (in vitro)

>80%

Endothelin-1—the peptide that constricts arteries—reduced to near-undetectable levels.

Petrangolini et al. 2021 · PMC7922661 · endothelial cell model

↓ Systolic BP · Benolea®

−11 pts

Reduction from baseline at 1,000mg daily over 8 weeks in borderline hypertensive identical twins.

Perrinjaquet-Moccetti et al. 2008 · monozygotic twin RCT · 8 weeks

↓ Systolic BP · Benolea® 

−11.5 pts

Systolic BP reduction in 8-week double-blind active-controlled study in 232 stage-1 hypertensive patients.

Susalit et al. 2011 · Phytomedicine · 232 patients · 8 weeks

Dual-ingredient mechanism 

Two polyphenols, two pathways

Pathway 1 · Vasodilation via Nitric Oxide

Pathway 1 · Vasodilation via nitric oxide

Enovita® Grape Seed Extract

OPC-rich · Champagne, France
300mg daily · 95% polyphenols · 85% OPCs

93% efficacy

BP normalized in 93% of 300mg group after 16 weeks. −37 pts systolic, −9 pts diastolic. Improved microcirculation. No side effects.

Belcaro 2013 · 119 patients · PMC3792515

+154% eNOS

Nitric oxide synthase enzyme activated 154% — relaxes and widens blood vessels. Endothelin-1 reduced to near-zero.

Petrangolini 2021 · HUVEC model ·  In vitro

↑ Microcirculation

Improved blood flow throughout capillary beds confirmed by laser Doppler flowmetry alongside blood pressure reduction.

Belcaro 2013 · LDF measurements

93% BP normalization rate

Pathway 2 · Vessel Tone via ACE Inhibition

Benolea® Olive Leaf Extract

Oleuropein-rich · Spanish olive trees
1,000mg daily · 16% oleuropein · 30% total polyphenols

−13 pts systolic

Systolic reduction at 1,000mg in identical twin RCT. More than double the benefit of 500mg dose. First improvements within 7 days.

Perrinjaquet-Moccetti 2008 · twin pairs

−11.5 pts systolic

Significant BP reduction in 8-week active-controlled study in 232 stage-1 hypertensive patients. LDL and triglycerides also reduced.

Susalit 2011 · 162 patients · double-blind · randomized

2× efficacy

The 1,000mg dose delivers more than double the systolic benefit of the 500mg dose most competitors use.

Dose-response confirmed across both trials

Beyond blood pressure

Additional cardiovascular benefits

Antioxidant Protection

Cholesterol & Lipids

↓ LDL + TG

Benolea® significantly reduced total cholesterol and triglycerides in the Susalit 2011 active-controlled study. OPCs from Enovita® also protect LDL from oxidation, a key mechanism in atherosclerotic plaque development.

Susalit 2011 (Benolea®) · Belcaro 2013 (oxidative stress markers)

Vascular Inflammation

Antioxidant Protection

↓ sICAM

Enovita® significantly reduced soluble ICAM-1 — a key marker of vascular wall inflammation linked to atherosclerotic plaque formation. Reduction in endothelin-1 further demonstrates anti-inflammatory action at the vessel wall level.

Petrangolini 2021 · endothelial cell model + human RCT markers

Antioxidant Protection

Antioxidant Protection

↓ Oxidative stress

OPCs from grape seed and oleuropein from olive leaf are among the most potent natural antioxidants studied. The Belcaro 2013 study confirmed significant improvements in plasma oxidative status alongside the blood pressure reductions.

Belcaro 2013 · plasma oxidative status confirmed by blood markers

Blood Sugar & Insulin

Antioxidant Protection

↓ Glucose

Oleuropein from olive leaf has been shown to support glucose metabolism and insulin sensitivity in research settings, consistent with the broader body of olive leaf clinical evidence.

Consistent with broader olive leaf + OPC research literature

Clinical References

Enovita® · Registry Study · Primary BP Evidence

Belcaro et al., PMC3792515 · 2013

Controlled registry study. 119 pre- and mildly hypertensive adults. 150mg and 300mg vs. lifestyle-only control. 16 weeks. 93% BP normalization at 300mg. −37 points systolic, −9 points diastolic. Improved microcirculation. No side effects. Compliance >94%.

119 patients · 16 weeks · 93% efficacy

Enovita® · Mechanism + Double-Blind RCT

Petrangolini et al., PMC7922661 · 2021

HUVEC endothelial cell study (in vitro) + randomized, double-blind, placebo-controlled human RCT in 80 mild-hypertensive adults. 300mg/day for 16 weeks. BP significantly modulated vs. placebo. eNOS +154% and endothelin-1 reduced to near-undetectable (in vitro mechanism).

80 adults · Double-blind · In vitro mechanism

Benolea® · Twin Study · Dose-Dependent

Perrinjaquet-Moccetti et al. · 2008

Randomized controlled trial in monozygotic twin pairs with borderline hypertension. 500mg vs. 1,000mg Benolea® for 8 weeks. Dose-dependent response: max −13 points systolic and −5 points diastolic at 1,000mg. LDL significantly reduced. Improvements within 7 days.

Identical twins · Dose-dependent · 8 weeks

Benolea® · Active-Controlled · Stage-1 Hypertension

Susalit et al., Phytomedicine 2011

Randomized, double-blind, active-controlled. 232 stage-1 hypertension patients. 8 weeks. Significant reduction in systolic (−11.5 pts) and diastolic (−4.8 pts) blood pressure. Additionally reduced total cholesterol and triglycerides.

232 patients · Active-controlled · Double-blind

Grape Seed Extract · Meta-Analysis Confirmation

Zhang et al., Medicine 2016

Meta-analysis of 16 randomized controlled trials on grape seed extract and blood pressure. Significant systolic BP reduction confirmed across studies. Validates the broader OPC mechanism across diverse formulations and populations.

16 RCTs · Systolic BP confirmed

Olive Leaf Extract · Meta-Analysis · 12 RCTs

Hadi et al. 2022

Systematic review and meta-analysis of 12 RCTs. Confirmed blood pressure and triglyceride reductions across independent studies — consistent with both Benolea® human trials and supporting generalizability of results.

819 participants · 12 RCTs

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*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. "Points" refers to mmHg, the standard unit of blood pressure measurement. The −37 point systolic and −9 point diastolic reductions and 93% BP normalization rate are from Belcaro et al. 2013 (119 pre/mildly hypertensive adults, 16 weeks, 300mg Enovita®, registry study with concurrent lifestyle intervention). The +154% eNOS activation and >80% endothelin-1 reduction are from in vitro endothelial cell experiments — they describe the vasodilation mechanism, not a measured human outcome. The −13 point systolic figure is from the Perrinjaquet-Moccetti 2008 twin RCT (1,000mg Benolea®, 8 weeks). The −11.5 point result is from Susalit et al. 2011 (232 stage-1 hypertensive patients, active-controlled, 8 weeks). All results are population-specific and individual results may vary.

Clinical References

Enovita® · Registry Study · Primary BP Evidence

Belcaro et al., PMC3792515 · 2013

Controlled registry study. 119 pre- and mildly hypertensive adults. 150mg and 300mg vs. lifestyle-only control. 16 weeks. 93% BP normalization at 300mg. −37 points systolic, −9 points diastolic. Improved microcirculation. No side effects. Compliance >94%.

119 patients · 16 weeks · 93% efficacy

Enovita® · Mechanism + Double-Blind RCT

Petrangolini et al., PMC7922661 · 2021

HUVEC endothelial cell study (in vitro) + randomized, double-blind, placebo-controlled human RCT in 80 mild-hypertensive adults. 300mg/day for 16 weeks. BP significantly modulated vs. placebo. eNOS +154% and endothelin-1 reduced to near-undetectable (in vitro mechanism).

80 adults · Double-blind · In vitro mechanism

Benolea® · Twin Study · Dose-Dependent

Perrinjaquet-Moccetti et al. · 2008

Randomized controlled trial in monozygotic twin pairs with borderline hypertension. 500mg vs. 1,000mg Benolea® for 8 weeks. Dose-dependent response: max −13 points systolic and −5 points diastolic at 1,000mg. LDL significantly reduced. Improvements within 7 days.

Identical twins · Dose-dependent · 8 weeks

Benolea® · Active-Controlled · Stage-1 Hypertension

Susalit et al., Phytomedicine 2011

Randomized, double-blind, active-controlled. 232 stage-1 hypertension patients. 8 weeks. Significant reduction in systolic (−11.5 pts) and diastolic (−4.8 pts) blood pressure. Additionally reduced total cholesterol and triglycerides.

232 patients · Active-controlled · Double-blind

Grape Seed Extract · Meta-Analysis Confirmation

Zhang et al., Medicine 2016

Meta-analysis of 16 randomized controlled trials on grape seed extract and blood pressure. Significant systolic BP reduction confirmed across studies. Validates the broader OPC mechanism across diverse formulations and populations.

16 RCTs · Systolic BP confirmed

Olive Leaf Extract · Meta-Analysis · 12 RCTs

Hadi et al. 2022

Systematic review and meta-analysis of 12 RCTs. Confirmed blood pressure and triglyceride reductions across independent studies — consistent with both Benolea® human trials and supporting generalizability of results.

819 participants · 12 RCTs

Ready to Try Durable
BLOOD PRESSURE?

Get Special Offer →

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. "Points" refers to mmHg, the standard unit of blood pressure measurement. The −37 point systolic and −9 point diastolic reductions and 93% BP normalization rate are from Belcaro et al. 2013 (119 pre/mildly hypertensive adults, 16 weeks, 300mg Enovita®, registry study with concurrent lifestyle intervention). The +154% eNOS activation and >80% endothelin-1 reduction are from in vitro endothelial cell experiments — they describe the vasodilation mechanism, not a measured human outcome. The −13 point systolic figure is from the Perrinjaquet-Moccetti 2008 twin RCT (1,000mg Benolea®, 8 weeks). The −11.5 point result is from Susalit et al. 2011 (232 stage-1 hypertensive patients, active-controlled, 8 weeks). All results are population-specific and individual results may vary.