Study of Osteopathic Manipulation in the Management of Angina
NCT ID: NCT00708279
Last Updated: 2011-04-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
1 participants
INTERVENTIONAL
2007-08-31
2008-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Osteopathic Manipulative Treatment for Back Pain
NCT03892759
Osteopathic Manipulative Medicine and Kinetics
NCT01376687
Effects of OMT on ANS: a Thermography Study
NCT03888456
The Effect of Osteopathic Treatment in Pain and Functionality Individuals With Chronic Neck Pain
NCT02956863
Physiological Responses to Osteopathic Manipulative Techniques in Healthy Young Adults
NCT05515926
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
A
After establishing a baseline for the first 4 weeks of trial involvement, thereby providing their own control group, all participants begin the intervention phase of osteopathic manipulation.
Osteopathic manipulation
Participant will be evaluated and treated for somatic dysfunction utilizing osteopathic manipulation once a week for 3 weeks, then once every 3 weeks for three more visits; a total of 6 interventions in 3 months.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Osteopathic manipulation
Participant will be evaluated and treated for somatic dysfunction utilizing osteopathic manipulation once a week for 3 weeks, then once every 3 weeks for three more visits; a total of 6 interventions in 3 months.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* documented coronary artery disease via previous myocardial infarction, abnormal stress test, or abnormal coronary angiogram of greater than or equal to 50% luminal obstruction of at least one epicardial vessel.
Exclusion Criteria
* symptomatic heart failure
* symptomatic aortic stenosis or any valvular disease
* significant pulmonary disease
* unstable angina
* major surgery or angioplasty in the past three months
* acute myocardial infarction within past three months
* insulin dependent diabetes mellitus
* uncontrolled hypertension
* acute renal or hepatic failure
* currently being treated with osteopathic manipulation
18 Years
81 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Osteopathic Heritage Foundations
OTHER
University of New England
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Edward Via College of Osteopathic Medicine
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Joy L. Palmer, D.O.
Role: PRINCIPAL_INVESTIGATOR
University of New England
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Health Care
Saco, Maine, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
F-07-04 AOA/OHF Fellowship
Identifier Type: OTHER
Identifier Source: secondary_id
F-07-04 SOMMA
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.