Coronary Blood Flow Regulation During General Anesthesia
NCT ID: NCT00866801
Last Updated: 2015-10-14
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
45 participants
OBSERVATIONAL
2009-04-30
2014-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
These disturbances in coronary blood flow may contribute to the development of myocardial ischemia in the perioperative period. Furthermore, patients with an intrinsically altered autonomic sympathetic innervation, like diabetics, are even more prone to develop perioperative disturbances in coronary blood flow.
Here the researchers will investigate what the direct effects are of general and locoregional anesthesia on the CBF. Furthermore, the researchers aim to evaluate whether diabetic subjects show more disturbed CBF responses to anesthesia as compared to non-diabetics.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effects of High Spinal Anesthesia on Heart Function, Stress Response and Pain Control in Aortic Valve Surgery
NCT00348920
Prospective Evaluation of Volatile Sedation After Heart Valve Surgery
NCT04958668
A Study of Changes in Heart Function and Blood Flow in People Receiving Anesthesia
NCT05954832
Heart Failure and Hemodynamic Stability During Anesthesia Induction
NCT03576261
Premedication and Haemodynamics After Spinal Anesthesia
NCT01066247
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Cardiac complications like myocardial ischemia remain one of the main causes of perioperative morbidity and mortality. Interestingly, the presence of cardiovascular autonomic neuropathy (CAN) strongly predicts abnormalities in myocardial perfusion and impaired coronary vasodilator responses to stress. This implies that symptoms of CAN, like resting tachycardia, orthostasis and alterations in heart rate variability may predict the degree of impairment of CBF regulation. Indeed, autonomic neuropathy as determined by heart rate variability predicted mortality in patients with coronary artery disease undergoing non-cardiac surgery, but the contribution of impaired coronary vasodilatory responses to these results has not been established. Clarification of the relation between autonomic control and CBF during anesthesia may not only contribute to our insight in pro-ischemic processes in the heart, but may lead to changes in preoperative assessment of patients at risk for perioperative ischemia, thereby reducing perioperative complications.
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.
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Healthy
Healthy subjects scheduled for general anesthesia
No interventions assigned to this group
Healthy with thoracic epidural anelgesia
Healthy subjects scheduled for general anesthesia and thoracic epidural analgesia
No interventions assigned to this group
Diabetes
Subjects with diabetes scheduled for general anesthesia
No interventions assigned to this group
Diabetes with autonomic neuropathy
Subjects with diabetes and cardiovascular autonomic neuropathy scheduled for general anesthesia
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* age between 18-75 years
* scheduled for non-cardiac intermediate or high risk surgery
* for patient group 2: indication for thoracic epidural anesthesia
Exclusion Criteria
* known/documented cardiac disease
* (untreated) hypertension
* abnormal ECG or echocardiogram
* peripheral vascular disease
* renal disease requiring hemo- or peritoneal dialysis
* inability to perform transthoracic echocardiography
* medication interfering with presynaptic catecholamine uptake
* for patient group 2: contra-indication for thoracic epidural anesthesia (bleeding diathesis, infection at the puncture site, patient refusal, severe stenotic valvular disease)
* previous allergic reaction to echocardiographic contrast agents
* contraindications for the use of echocardiographic contrast agents
18 Years
75 Years
MALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Netherlands Heart Foundation
OTHER
Amsterdam UMC, location VUmc
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
C.S.E. Bulte
MD
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Carolien SE Bulte, MD
Role: PRINCIPAL_INVESTIGATOR
Amsterdam UMC, location VUmc
R. A. Bouwman, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Amsterdam UMC, location VUmc
C. Boer, PhD
Role: STUDY_CHAIR
Amsterdam UMC, location VUmc
S. A. Loer, MD, PhD, MSC
Role: STUDY_DIRECTOR
Amsterdam UMC, location VUmc
O. Kamp, MD, PhD
Role: STUDY_CHAIR
Amsterdam UMC, location VUmc
M. Diamant, MD, PhD
Role: STUDY_CHAIR
Amsterdam UMC, location VUmc
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
VU University Medical Center
Amsterdam, North Holland, Netherlands
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Bulte CS, van den Brom CE, Loer SA, Boer C, Bouwman RA. Myocardial blood flow under general anaesthesia with sevoflurane in type 2 diabetic patients: a pilot study. Cardiovasc Diabetol. 2014 Mar 23;13:62. doi: 10.1186/1475-2840-13-62.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2008 T003
Identifier Type: -
Identifier Source: secondary_id
ANES 2008-12
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.