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Coenzyme Q-10 and Pulmonary Arterial Hypertension

Primary Purpose

Pulmonary Arterial Hypertension

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Coenzyme Q-10 in Pulmonary Hypertension subjects
Coenzyme Q-10 in Normal Control subjects
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Arterial Hypertension focused on measuring Coenzyme Q-10, Pulmonary Arterial Hypertension, Pulmonary Arterial Hypertension Class I (Venice 2003)

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Males and Females age equal to or greater than 18 not to exceed 65.
  • Patients with PAH Class 1 (Venice 2003)
  • PAH medications must not have changed for the last two months.
  • Women of child-bearing age must use a double-barrier local contraception until completion of study.
  • Subjects must demonstrate understanding of study and sign informed consent and have a reliable method of communication for contact and the ability to comply with the study requirements.

Exclusion Criteria:

  • Participation in any other studies at the time of enrollment
  • History of any significant illness within four weeks of starting Coenzyme Q-10
  • Hepatic insufficiency (transaminase levels >4 fold the upper limit of normal or bilirubin >2 fold the upper limit of normal).
  • Renal insufficiency (creatinine >2)
  • Pregnancy,breast-feeding or lack of safe contraception.
  • Acute heart failure
  • Known allergy to the study drug or drugs similar to the study drug
  • History of drug or alcohol abuse within last 12 months

Sites / Locations

  • Cleveland Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Coenzyme Q 10 and Pulmonary Hypertension

Coenzyme Q 10 and Normal Controls

Arm Description

PAH subjects to take Co-Q daily for three months

Normal controls to take Co-Q daily for three months

Outcomes

Primary Outcome Measures

Left Ventricular End Diastolic Volume
Amount of blood in ventricle at end of diastole
Right Ventricular Outflow
Velocity time interval
Right Ventricle Myocardial Performance
Tei Index=(IRT+ICT)/ET, where IRT is isovolumic
Tricuspid Regurgitation Grade
Tricuspid Regurgitation Grade ranges from 1 (normal) to 4 (severe regurgitation)
Right Atrial Pressure

Secondary Outcome Measures

Red Blood Cells
Hemoglobin
Hematocrit
Mean Corpuscular Hemoglobin
Red Blood Cell Distribution Width

Full Information

First Posted
March 19, 2010
Last Updated
March 19, 2015
Sponsor
The Cleveland Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT01148836
Brief Title
Coenzyme Q-10 and Pulmonary Arterial Hypertension
Official Title
Coenzyme Q-10 in the Treatment of Pulmonary Arterial Hypertension
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Cleveland Clinic

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effects of Coenzyme Q-10, an antioxidant, in the treatment of pulmonary hypertension.
Detailed Description
Abnormalities in the blood vessels in the lung are the hallmark of pulmonary hypertension. Links between increased free radical production, mitochondrial dysfunction and pulmonary hypertension have been studied but are poorly understood. The mitochondria of cells is the location where cellular energy is created and free radicals are atoms or groups of atoms with an odd (unpaired) number of electrons and can be formed when oxygen interacts with certain molecules. Once formed these reactive radicals can start a chain reaction, like dominoes. Their chief danger comes from the damage they can do when they react with important cellular components. Cells may function poorly or die if this occurs. The body produces free radicals in the normal course of energy production and in pulmonary hypertension, free radical production is found to be increased. To prevent free radical damage the body has a defense system of antioxidants. Coenzyme Q-10 is an antioxidant and it helps to protect cells from damage caused by the body's own free radicals. By providing oral supplementation of coenzyme Q-10, free radical levels will be decreased and cellular functioning in the pulmonary blood vessels may improve and even return to near normal functioning. The purpose of this study is to evaluate the effects of coenzyme Q-10, an antioxidant, in the treatment of pulmonary hypertension. We will assess coenzyme Q-10 supplementation in the treatment of pulmonary hypertension by clinical measurements and blood levels of certain cellular components. We would like to assess the effects of coenzyme Q-10 on the pulmonary vessels by measuring the lung diffusing capacity (a breathing test) and exhaled Nitric Oxide (NO) (a substance in the body that relaxes or dilates blood vessels). We will also measure endothelial progenitor cells (cells from the bone marrow) from a blood sample; these cells are markers of measure of blood vessel formation and repair. We will also measure the activity of superoxide dismutase (a protein in cells that executes the breakdown of a free radical into oxygen and hydrogen peroxide) in the blood. In addition, we will measure levels of coenzyme Q-10 in the blood. Other markers of disease response to therapy will be done including physical exam, BNP level (a blood marker that correlates with heart function), 6-minute walk and echocardiography (ultrasound of the heart). A total of 60ml (5 tablespoons) of blood will be drawn at each visit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Arterial Hypertension
Keywords
Coenzyme Q-10, Pulmonary Arterial Hypertension, Pulmonary Arterial Hypertension Class I (Venice 2003)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Coenzyme Q 10 and Pulmonary Hypertension
Arm Type
Experimental
Arm Description
PAH subjects to take Co-Q daily for three months
Arm Title
Coenzyme Q 10 and Normal Controls
Arm Type
Experimental
Arm Description
Normal controls to take Co-Q daily for three months
Intervention Type
Dietary Supplement
Intervention Name(s)
Coenzyme Q-10 in Pulmonary Hypertension subjects
Other Intervention Name(s)
Coenzyme Q: Nutritional Supplement
Intervention Description
Take 100mg Co-Q for three times daily
Intervention Type
Dietary Supplement
Intervention Name(s)
Coenzyme Q-10 in Normal Control subjects
Intervention Description
Take 100mg Co-Q for three times daily
Primary Outcome Measure Information:
Title
Left Ventricular End Diastolic Volume
Description
Amount of blood in ventricle at end of diastole
Time Frame
before and after three months of CoQ
Title
Right Ventricular Outflow
Description
Velocity time interval
Time Frame
before and after three months of CoQ
Title
Right Ventricle Myocardial Performance
Description
Tei Index=(IRT+ICT)/ET, where IRT is isovolumic
Time Frame
before and after three months of CoQ
Title
Tricuspid Regurgitation Grade
Description
Tricuspid Regurgitation Grade ranges from 1 (normal) to 4 (severe regurgitation)
Time Frame
before and after three months of CoQ
Title
Right Atrial Pressure
Time Frame
before and after three months of CoQ
Secondary Outcome Measure Information:
Title
Red Blood Cells
Time Frame
before and after three months of CoQ
Title
Hemoglobin
Time Frame
before and after three months of CoQ
Title
Hematocrit
Time Frame
before and after three months of CoQ
Title
Mean Corpuscular Hemoglobin
Time Frame
before and after three months of CoQ
Title
Red Blood Cell Distribution Width
Time Frame
before and after three months of CoQ

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Males and Females age equal to or greater than 18 not to exceed 65. Patients with PAH Class 1 (Venice 2003) PAH medications must not have changed for the last two months. Women of child-bearing age must use a double-barrier local contraception until completion of study. Subjects must demonstrate understanding of study and sign informed consent and have a reliable method of communication for contact and the ability to comply with the study requirements. Exclusion Criteria: Participation in any other studies at the time of enrollment History of any significant illness within four weeks of starting Coenzyme Q-10 Hepatic insufficiency (transaminase levels >4 fold the upper limit of normal or bilirubin >2 fold the upper limit of normal). Renal insufficiency (creatinine >2) Pregnancy,breast-feeding or lack of safe contraception. Acute heart failure Known allergy to the study drug or drugs similar to the study drug History of drug or alcohol abuse within last 12 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jackie Sharp, CNP
Organizational Affiliation
The Cleveland Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States

12. IPD Sharing Statement

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Coenzyme Q-10 and Pulmonary Arterial Hypertension

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