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Autonomic Function Testing for Heart Condition
N/A
Waitlist Available
Led By C. Noel Bairey Merz, M.D.
Research Sponsored by Cedars-Sinai Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours
Awards & highlights
Study Summary
This trial is investigating the role of the autonomic nervous system in microvascular coronary dysfunction, a condition that affects small arteries in the heart and causes chest pain. They will recruit 100 participants over the next five years.
Who is the study for?
This trial is for women over 18 with microvascular coronary dysfunction (MCD) and persistent chest pain, but no obstructive coronary artery disease. They must be able to consent and not have conditions like severe asthma, heart block, or metal devices in the chest that would exclude them from certain tests.Check my eligibility
What is being tested?
The study investigates how the autonomic nervous system responds to stress in women with MCD. It involves non-invasive tests like RESPeRATE breathing, SPECT cardiac scans, mental stress testing, PAT testing, and HRV measurement to assess cardiovascular reactivity.See study design
What are the potential side effects?
Potential side effects are minimal as most interventions are non-invasive monitoring techniques. However, there may be discomfort or minor risks associated with the SPECT scan due to radiation exposure and possible allergic reactions to injected tracers.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Cardiovascular Reactivity (CVR)
Trial Design
3Treatment groups
Experimental Treatment
Group I: normal reference controlsExperimental Treatment5 Interventions
40 normal reference controls subjects Visits 1 and 2
Group II: abnormal CRTExperimental Treatment5 Interventions
40 subjects with microvascular coronary dysfunction (MCD) defined as abnormal CRT.
Visits 1, 2, and 3
Group III: Cardiac Syndrome XExperimental Treatment5 Interventions
20 subjects with symptoms and normal stress tests, no MCD. Visits 1 and 2
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Who is running the clinical trial?
Cedars-Sinai Medical CenterLead Sponsor
499 Previous Clinical Trials
164,752 Total Patients Enrolled
6 Trials studying Nephrotic Syndrome
592 Patients Enrolled for Nephrotic Syndrome
C. Noel Bairey Merz, M.D.Principal InvestigatorCedars-Sinai Medical Center
2 Previous Clinical Trials
188 Total Patients Enrolled
Puja Mehta, M.D.Principal InvestigatorEmory University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: abnormal CRT
- Group 2: Cardiac Syndrome X
- Group 3: normal reference controls
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is the enrollment period for this trial still open?
"Clinicaltrials.gov accounts for this clinical trial no longer seeking volunteers, with the initial posting being on February 1st 2011 and the last edit occurring July 20th 2022. Fortunately, there are still 29 other medical trials actively recruiting participants at present."
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