Recruiting PHASE1 Hypertension

New treatment option for Hypertension

Official title Metabolic Imaging of the Heart Using Hyperpolarized (13C) Pyruvate Injection

ClinicalTrials.gov ID: NCT02648009

What this study is testing

What is Hyperpolarized (13) Pyruvate Injection?

Hyperpolarized (13) Pyruvate Injection is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for hypertension.

Also referred to as Hyperpolarized Pyruvate (13) Injection.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
The prevalence of congestive heart failure (CHF) in Canada is high, representing one of the health care system's most expensive diagnoses. Despite major advances in medicine, the mortality and morbidity from CHF remains great.
  • Phase 1: an early, usually small safety study

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 19 to 75. Healthy volunteers may be eligible.

You may be able to join if

  • Written consent
  • Age: 19 to 50 in Arm 1, 30 to 75 in Arm 2
  • Group 2A and 2E participants have left-ventricular hypertrophy
  • Group 2B and 2F participants have diagnosed hypertrophic cardiomyopathy
  • Group 2C and 2G participants are stable outpatients with NYHA class 1-3 heart failure with evidence of elevated LV mass (LVH), irrespective of LVEF.

You likely can't join if

  • Contraindications to MRI or MRI contrast agents
  • Hemoglobin ≤ 9.0 gm/dL (only Group 2 participants)
  • Glomerular filtration rate (based on MDRD Equation) \< 30 ml/min/1.73m2 (only Group 2 participants)
  • Any condition leading to a life expectancy \<1 year
  • Medically diagnosed claustrophobia
  • Have received, or are scheduled to receive, another investigational medicinal product from 1 month prior to 1 month after inclusion in this study
See the full eligibility criteria
Who can join
  • Written consent
  • Age: 19 to 50 in Arm 1, 30 to 75 in Arm 2
  • Group 2A and 2E participants have left-ventricular hypertrophy
  • Group 2B and 2F participants have diagnosed hypertrophic cardiomyopathy
  • Group 2C and 2G participants are stable outpatients with NYHA class 1-3 heart failure with evidence of elevated LV mass (LVH), irrespective of LVEF.
  • Group 2D and 2H participants are stable patients with type 2 DM who have a HcA1c between 6.5-9% on oral hypoglycemic agents
What rules you out
  • Contraindications to MRI or MRI contrast agents
  • Hemoglobin ≤ 9.0 gm/dL (only Group 2 participants)
  • Glomerular filtration rate (based on MDRD Equation) \< 30 ml/min/1.73m2 (only Group 2 participants)
  • Any condition leading to a life expectancy \<1 year
  • Medically diagnosed claustrophobia
  • Have received, or are scheduled to receive, another investigational medicinal product from 1 month prior to 1 month after inclusion in this study
  • BMI of less than 18.5 or greater than 32
  • Group 1: medically diagnosed heart disease

The study team makes the final eligibility decision.

Where it's taking place

  • Toronto, Ontario, Canada

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 19 years to 75 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Toronto, Ontario, Canada. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.