Clinical Trials Logo

Clinical Trial Summary

A coronary chronic total occlusion refers to the long term complete blockage of a blood vessel supplying the heart. Exercise is beneficial for patients with heart problems, including people with narrowed blood vessels. However, exercise has not previously been tested in patients with a completely blocked blood vessel. Therefore, the aim of this study is to evaluate exercise testing in participants with a coronary chronic total occlusion, and to see if the physiological changes that occur are reproducible when participants are re-tested. Secondly, the study will see if sustained exercise is safe in this population. Participants will make 3 visits to our Laboratory. During the first two visits participants will complete symptom limited exercise tests using a stationary bike for approximately 8-12 minutes. The bikes' resistance will gradually increase until participants choose to stop or the researcher ends the test. Participants will wear a mask that collects exhaled breath for testing, and will be connected to an electrocardiogram (heart trace monitor), and blood pressure cuff for monitoring throughout the test. During visits one and three patients will also have blood taken pre and post exercise. Researchers will analyse how the amount of oxygen consumed with increasing exercise relates to the participants' heart rate. A plateau in these measures would indicate a change in the heart's blood supply resulting in reduced function. The participants' third visit will involve cycling under the same conditions as previous visits. However, during this test participants will be asked to cycle continuously for 20 minutes at a resistance set by the researchers. This level of resistance is determined from the results of the first test, as the point at which changes in blood flow and heart function occurred. In the last five minutes of the test patients will have an echocardiogram (heart scan), to look at the heart function.


Clinical Trial Description

The main purpose of this research will be to investigate whether or not changes in the heart's blood supply and function can be seen in coronary chronic total occlusion patients, by investigating information collected during a cardiopulmonary exercise test. Secondly, can these patients exercise safely at this level for an extended period of time. The cardiology department at Castle Hill Hospital treats approximately 40 patients each year who have a single chronic total coronary occlusion. Researchers will recruit 12 consecutive patients who have a complete blockage of one of the major blood vessels to the heart. These recruits will be found either when the diagnosis is made (during a coronary angiogram when dye is injected into the heart blood vessels), or from the dedicated departmental database at Castle Hill Hospital. Patients will be identified by a member of their usual clinical team. Potential participants will be given a patient information leaflet, explaining the aims of the research and what the study involves. A minimum of 48 hours later, patients will be given a follow up call by a member of their usual clinical care team. During this call if patients are interested in participating they will be asked for their verbal consent to be contacted by the research team, and given the opportunity to ask questions about the study. Patients will then be invited to attend Castle Hill Hospital to discuss the trial in more detail. Patients will be given the chance to ask questions and explain any concerns they have about the research. They will also be reminded that inclusion in the research is voluntary, and that they can choose to leave the study at any time. Once informed consent has been obtained by a member of the research team, participants will proceed with the baseline assessment (Visit 1). Questions will then be asked about their previous medical history, current condition, and medications they are taking. Basic information will also be collected from the participants; such as height, weight, resting heart rate, blood pressure, ECG, (to measure the electrical activity of the heart), echocardiogram (ultrasound imaging of the hearts function, involving gel being placed on the chest and a hand-held device pressed to the area), and a pre-test blood sample. Following these measures, the participant will be asked to ride a stationary bike against increasing resistance until they can no longer continue (approx. 8-12 minutes). During this exercise they will have their exhaled air (collected via mask), heart rate, blood pressure, and electrocardiogram measured throughout. After completing the test a final blood sample will be collected. After a minimum of 72 hours and a maximum of 2 weeks, participants will be invited back for visit 2. This visit will include a brief health assessment and will otherwise follow the same structure as the previous visit, minus the blood samples pre and post exercise, and resting echocardiogram (heart scan). The purpose of the second visit is to see if the results of the test are reproducible. The main aim of the test is to see if there is a point that can be identified when the heart is no longer able to work any harder. In healthy individuals, as they cycle harder, the oxygen taken from the lungs with each heartbeat would gradually increase. This would be visible to the researchers in the results of the test. When the body is working hard the heart is forced to work hard too. It does this by increasing its stroke volume, which is the amount of blood it squeezes out to the body with each beat. If the stroke volume increases then the amount of oxygen taken each heart beat will increase. If the participant in the test is a patient with a coronary chronic total occlusion then the research team expect that this will not follow the same path. Under normal conditions like sitting, standing, walking and perhaps light cycling it is possible for this patient's heart to supply enough blood to the muscles. However, because the heart itself is a muscle it too needs more oxygen and therefore more blood if it is going to work harder. As the participant exercises, the heart will try to increase it's stroke volume to supply more oxygen. Unfortunately, because the heart has a blocked vessel it will not receive enough blood to be able to increase its stroke volume. Therefore, the amount of oxygen taken each beat will not increase beyond a certain point, and the researchers should see this as a flattening in the results of the test. The research team will use the data collected from the first and second visit to see if this flattening point exists for each participant. If this point is seen in both tests the researcher will prescribe exercise at this level for the third visit. A minimum of 72 hours and a maximum of 2 weeks after visit 2, patients will be invited back for their third and final visit. This visit will again begin with a brief health assessment before measures of resting heart rate, blood pressure, electrocardiogram, and a blood sample are collected. Participants will then be asked to pedal a stationary bike this time at a personalised resistance for 20 minutes, whilst exhaled gas, heart rate, blood pressure and electrocardiogram are monitored. During the final 5 minutes of exercise the participant will be given a stress echocardiogram (ultrasound scan of the heart). As in visit 1 a blood sample will be taken from the participant after exercise has been completed. All visits will occur within the department of Cardiology at Castle Hill Hospital. This is a pilot study and therefore, the number of participants has been determined based on previous experience of performing these tests on patients with non-occlusive coronary disease. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03993522
Study type Interventional
Source University of Hull
Contact
Status Terminated
Phase N/A
Start date June 1, 2019
Completion date December 1, 2022

See also
  Status Clinical Trial Phase
Completed NCT01721096 - XIENCE PRIME Japan Post-Marketing Surveillance (PMS)
Completed NCT00987610 - Guidewire for Chronic Total Occlusion Phase 4
Completed NCT02533128 - Biomarkers, Blood Pressure, BIS: Risk Stratification/Management of Patients at Cardiac Risk in Major Noncardiac Surgery N/A
Completed NCT04246125 - Patient Skin Dose in Interventional Radiology
Completed NCT03717675 - Supplemental Study to Evaluate the Safety and Effectiveness of the NovaCross™ Micro-catheter N/A
Recruiting NCT03588481 - IRIS- DESyne X2 in the IRIS-DES Registry
Recruiting NCT05089864 - STAR and Deferred Stenting Study N/A
Not yet recruiting NCT03719014 - Cohort B of the Pivotal Study to Evaluate the Safety and Effectiveness of the NovaCross™ Micro-catheter N/A
Not yet recruiting NCT02963584 - Decision Aid in Chronic Total Occlusion (CTO) Patients N/A
Completed NCT00793221 - Non-acute Coronary occlusIon Treated By Everolimus ELuting Stent Phase 3
Completed NCT04281212 - Observational Study Evaluating the Management of Chronic Coronary Occlusions In France
Not yet recruiting NCT04562142 - A Novel Non-Invasive Acoustic Diagnostic for the Diagnosis of Coronary Artery Disease The CAD-det Validation Study N/A
Enrolling by invitation NCT02931331 - Coronary Revascularization Assessed by Stress PET N/A
Terminated NCT02683356 - Optical Coherence Tomography to Improve Outcome for Coronary Revascularisation Using Bioresorbable Vascular Scaffolds N/A
Completed NCT00657436 - Myeloid-Related Protein in Evaluation of Acute Chest Pain in the Emergency Departement N/A
Not yet recruiting NCT05848232 - Single-Arm Study Evaluating Use of the CORA Catheters for the Crossing of Coronary Chronic Total Occlusions Phase 3
Not yet recruiting NCT03159650 - Comparative Study Between Intravascular Ultrasonography Guided and Angiography-guided Recanalization of Coronary Chronic Total Occlusions N/A
Recruiting NCT02325869 - Clinical Study Protocol - Debris Interventional Removal in ACS (DESIRE-ACS) N/A
Completed NCT00640068 - Advanced Cardiovascular Imaging Consortium N/A
Completed NCT01759290 - ABSORB FIRST is a Registry Designed to Evaluate the Safety and Performance of Absorb Bioresorbable Vascular Scaffold (Absorb BVS) Used in Real-world Patients. N/A