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Oral Nitrite Trial for Hypertension and Metabolic Syndrome (ONPC)

Primary Purpose

Metabolic Syndrome, Hypertension

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
14 Nitrogen (N) Sodium Nitrite
Placebo
Sponsored by
Gladwin, Mark, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-60 years
  • Body mass index (BMI) ≥ 30 kg/m2
  • Hypertension: defined as systolic blood pressure ≥130 and/or diastolic blood pressure ≥85 mm Hg
  • Waist circumference: >102 cm in men, >88 cm in women

Exclusion Criteria:

  • Positive urine pregnancy test or breastfeeding
  • Concurrent use of medications affecting glucose metabolism (oral hypoglycemics, insulin, atypical antipsychotics)
  • Recent addition or change in dosing of hormonal contraceptive medications (Oral Contraceptive Pill (OCP), Intra Uterine Device (IUD), DepoProvera shot)
  • Current use of ≥3 anti-hypertensive agents regardless of blood pressure control or normotensive on a single or double agent
  • Current use of phosphodiesterase-5 (PD) inhibitors or organic nitrates. We will not exclude for dietary sources of nitrate/nitrite.
  • Not stable on treatments for the prior three months or not planning to remain on current dose of medications for blood pressure, contraception, etc.
  • Known chronic psychiatric or medical conditions including diabetes, liver or kidney disease or obesity syndromes
  • Thyroid Stimulating Hormone (TSH) >8 milli-International unit/mL
  • Smoker
  • Anemia (central lab hemoglobin < 11g/dL)
  • Active periodontal disease

Sites / Locations

  • Montefiore Hospital of UPMC

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Active drug

Placebo

Arm Description

14 Nitrogen (N) Sodium Nitrite 40mg three times daily (TID)

placebo capsules three time daily (TID)

Outcomes

Primary Outcome Measures

Change in insulin sensitivity (i.e. insulin stimulated glucose disposal)
obtained by hyperinsulinemic euglycemic clamp

Secondary Outcome Measures

Change in systolic blood pressure
ambulatory blood pressure
Change in mean arterial pressure
ambulatory blood pressure
Change in diastolic blood pressure
ambulatory blood pressure
Change in methemoglobin level
by co-oximetry

Full Information

First Posted
August 5, 2015
Last Updated
April 13, 2021
Sponsor
Gladwin, Mark, MD
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1. Study Identification

Unique Protocol Identification Number
NCT02517697
Brief Title
Oral Nitrite Trial for Hypertension and Metabolic Syndrome
Acronym
ONPC
Official Title
Nitrite Modulation of Hypertension, Platelet Activation, and Endothelial and Mitochondrial Function
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Withdrawn
Why Stopped
We will not initiate recruitment for this protocol due to lack of funding to support this placebo-controlled trial.
Study Start Date
October 2020 (Anticipated)
Primary Completion Date
April 13, 2021 (Actual)
Study Completion Date
April 13, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Gladwin, Mark, MD

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of the study is to investigate effects of inorganic sodium nitrite on the cardiometabolic and hormonal disturbances observed in a targeted population of overweight/obese adults with metabolic syndrome and hypertension, at risk for insulin resistance and endothelial dysfunction.
Detailed Description
Cardiovascular disease remains the leading cause of death in the United States and worldwide. Several studies have demonstrated that fruit and vegetable rich diets significantly reduced blood pressure and reduced the risk of ischemic stroke and cardiovascular disease in general, the exact mechanisms remain poorly understood. Preclinical and clinical research over the last decade has revealed the important vasoprotective effects of nitrates and nitrites with regards to reduction in blood pressure, vascular inflammation and endothelial dysfunction. More recent findings suggest that inorganic nitrate and nitrite therapy may be involved in the regulation of glucose-insulin homeostasis. For this reason, development of an oral formulation of nitrite salt represents a rational avenue of exploration for the treatment of cardiovascular diseases, whereby nitrite would ensure rapid acting effects upon absorption. Nitrite could then be oxidized to nitrate via the enterosalivary circulation pathway. In this pathway, about 25% of circulating nitrate is concentrated in the saliva and reduced to nitrite by commensal mouth bacteria with nitrate reductase enzymes. The proposal will investigate the inorganic nitrite effects (in any form) on insulin sensitivity in a targeted population of overweight/obese adults with metabolic syndrome and hypertension, at risk for insulin resistance and endothelial dysfunction. This will be the third human trial using orally delivered nitrite (previously as aqueous solution).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome, Hypertension

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active drug
Arm Type
Experimental
Arm Description
14 Nitrogen (N) Sodium Nitrite 40mg three times daily (TID)
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
placebo capsules three time daily (TID)
Intervention Type
Drug
Intervention Name(s)
14 Nitrogen (N) Sodium Nitrite
Other Intervention Name(s)
sodium nitrite
Intervention Description
oral formulation of sodium nitrite 40 mg three times daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
oral formulation of matching placebo three times daily for 12 weeks
Primary Outcome Measure Information:
Title
Change in insulin sensitivity (i.e. insulin stimulated glucose disposal)
Description
obtained by hyperinsulinemic euglycemic clamp
Time Frame
baseline and 12 weeks
Secondary Outcome Measure Information:
Title
Change in systolic blood pressure
Description
ambulatory blood pressure
Time Frame
baseline and 12 weeks
Title
Change in mean arterial pressure
Description
ambulatory blood pressure
Time Frame
baseline and then biweekly throughout the 12 week treatment
Title
Change in diastolic blood pressure
Description
ambulatory blood pressure
Time Frame
baseline and 12 weeks
Title
Change in methemoglobin level
Description
by co-oximetry
Time Frame
baseline and then biweekly throughout the 12 week treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-60 years Body mass index (BMI) ≥ 30 kg/m2 Hypertension: defined as systolic blood pressure ≥130 and/or diastolic blood pressure ≥85 mm Hg Waist circumference: >102 cm in men, >88 cm in women Exclusion Criteria: Positive urine pregnancy test or breastfeeding Concurrent use of medications affecting glucose metabolism (oral hypoglycemics, insulin, atypical antipsychotics) Recent addition or change in dosing of hormonal contraceptive medications (Oral Contraceptive Pill (OCP), Intra Uterine Device (IUD), DepoProvera shot) Current use of ≥3 anti-hypertensive agents regardless of blood pressure control or normotensive on a single or double agent Current use of phosphodiesterase-5 (PD) inhibitors or organic nitrates. We will not exclude for dietary sources of nitrate/nitrite. Not stable on treatments for the prior three months or not planning to remain on current dose of medications for blood pressure, contraception, etc. Known chronic psychiatric or medical conditions including diabetes, liver or kidney disease or obesity syndromes Thyroid Stimulating Hormone (TSH) >8 milli-International unit/mL Smoker Anemia (central lab hemoglobin < 11g/dL) Active periodontal disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kara S Hughan, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mark Gladwin, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Study Director
Facility Information:
Facility Name
Montefiore Hospital of UPMC
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Oral Nitrite Trial for Hypertension and Metabolic Syndrome

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