- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01423422
Effects of Low Frequency Magnetic Field on Exercise Induced Angina
August 25, 2011 updated by: Aerotel Ltd
Effects of Low Frequency Electromagnetic Field on Patients With Exercise Induced Angina
The investigators have previously shown that a frequency of 15.95-16.00
Hz protects against acute myocardial infarction in rats.
In the current study the investigators would like to investigate whether this frequency enables cardiac patients with exercise-induced chest pain to exercise at higher workload and heart rate.
Therefore, patients will undergo two exercise stress tests, one test after being exposed to 30 minutes of the above mentioned frequency and another test after being exposed to sham (no frequency is turned ON).
The investigators will measure changes in the electrocardiogram (ECG), workload, exercise time, and subjective measure of chest pain (angina).
Study Overview
Status
Unknown
Conditions
Detailed Description
Several studies have shown that low frequency electromagnetic field has biological and therapeutic potential on the human body, however, to very limited extent on the heart.
In the current study cardiac patients suffering from exercise-induced-angina will undergo two consecutive stress tests, one test after being exposed for 30 minutes to the magnetic field and the other test after being exposed to placebo (magnetic field not operated).
The order of which the magnet will be operated will be randomly assigned for the patients so a group of patients will be exposed to the magnetic field at their first stress test and another groups of patients will be exposed to the magnetic field at their second stress test.
During resting period, and while the patients are subjected to the magnetic field, a 12 lead electrocardiogram (ECG) will be monitored.
Thereafter the magnetic field and frequency will be turned off and the patients will be subjected to graded exercise stress test during which they will be monitored for ECG and blood pressure changes.
Similar monitoring will be documented during the recovery period following the stress test.
In addition, the patients will grade their angina score as documented during the stress test.
The data will be compared between the two stress tests and to document any advantageous of the magnetic field on exercise time, workload, ECG changes and/or chest pain.
Study Type
Observational
Enrollment (Anticipated)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Tel-Hashomer, Israel, 52621
- Cardiac Rehabilitation Institute, sheba Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
35 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients enrolled at the Cardiac Rehabilitation Institute, sheba Medical Center
Description
Inclusion Criteria:
Patients with known exercise-induced-angina
Exclusion Criteria:
Patients that changed treatment course between the two exercise stress tests Patients that decided to drop from the second exercise stress test
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Frequency exposed patients
Patients exposed to the magnetic field with the specific frequency
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exercise workload for a given ECG change
Time Frame: within a month from the second exercise stress test
|
Exercise workload wil be compared between the two tests and according with the ECG changes recorded at these two tests.
|
within a month from the second exercise stress test
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Angina scale
Time Frame: Within a month from the last exercise stress test
|
Define the angina scale obtained between the two tests at a given workload.
|
Within a month from the last exercise stress test
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Ilan Hai, MD, Cardiac Rehabilitation Institute, sheba Medical Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2011
Primary Completion (Anticipated)
May 1, 2012
Study Completion (Anticipated)
October 1, 2012
Study Registration Dates
First Submitted
August 24, 2011
First Submitted That Met QC Criteria
August 25, 2011
First Posted (Estimate)
August 26, 2011
Study Record Updates
Last Update Posted (Estimate)
August 26, 2011
Last Update Submitted That Met QC Criteria
August 25, 2011
Last Verified
August 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- frequency medicine for angina
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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