- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05774535
Prospective, Observational Study on the Carotid Intima-media Thickness in Patients Undergoing Thyroid Surgery (TIROVASC)
Prospective, Observational Study on the Investigation of the Carotid Intima-media Thickness in Patients Undergoing Thyroid Surgery
The evaluation of carotid intima-media thickness (cIMT) has become a possible predictor of the future risk of cardiovascular diseases (CVD). Evidence to date shows that cIMT augmentation is correlated with the extent of atherosclerosis in the coronary arteries and with other risk factors for CVD. More recently, several studies have evaluated the association of cIMT with stroke, to determine whether this measure can also predict future cardiovascular events.
Although the published evidence is scarce and fragmentary, the cIMT retains an increasingly interesting role as a marker of atherosclerotic pathology.
The purpose of the study is to analyze cIMT in patients undergoing thyroidectomy to evaluate a possible correlation between the cIMT variation after the procedure and the cause of the thyroid disease, the levels of thyroid hormones, and the lipid or other markers of atherosclerosis levels.
The primary endpoint will be the variation of the measure of the cIMT before and after surgery.
Secondary endpoints will be:
- major cardiovascular adverse events (death, major stroke, minor stroke, transient ischemic attack) in the short-term period (≤30 days after the procedure);
- major cardiovascular adverse events (death, major stroke, minor stroke, transient ischemic attack) in the long-term period (>30 days after the procedure);
- the technical success of the procedure;
- the rate of postoperative complications. To date, there are no data that differentiate patients based on the causes of thyroid disease. The results of the present study will allow for correlating the variation of the cIMT to the causes of thyroid disease, the levels of thyroid hormones, and the levels of lipid and other markers of atherosclerosis.
Results from the present study may provide insights into possible areas of quality improvement. It may also influence the economic impact associated with carotid revascularization techniques, in terms of hospital charges and discharges to skilled nursing and rehabilitation facilities.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Contacts and Locations
Study Locations
-
-
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Milan, Italy, 20145
- Istituto Auxologico Italiano , IRCCS
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients undergoing thyroidectomy according to the American Thyroid Association (ATA), International neural monitoring study group guideline (INMSG), Italian Society of Endocrine Surgery (SIUEC);
- subjects who have read and signed the informed consent;
- subjects who undertake to undergo the instrumental examinations and visits necessary for the study during the follow-up;
- >18 years of age.
Exclusion Criteria:
- occlusion or stenosis of at least one carotid artery, with plaque > 30%;
- exposure to ionizing radiation;
- previous neck, carotid (endarterectomy or stenting) and/or thyroid surgery;
- clinical conditions that preclude proper follow-up;
- HIV, dialysis therapy and all clinical conditions with increased cIMT;
- uncontrolled dyslipidemia;
- pregnant and breastfeeding women;
- terminal patients.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Experimental
Patients who will undergo thyroidectomy
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Patients will undergo thyroidectomy according to the guidelines American Thyroid Association (ATA), Randolph. The following assessments will be performed within 10 days before the thyroidectomy procedure:
The following assessments will be performed after 30 days, 6 months and 12 months from the thyroidectomy procedure:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in Carotid Intima-Media Thickness (cIMT)
Time Frame: Baseline (10 days before the surgery), 30 days, 6 months and 12 months after the surgery
|
cIMT is a measurement of the thickness of tunica intima and tunica media, the innermost two layers of the wall of an artery.
The measurement is made by external ultrasound according to the recommendation of the Joint Carotid Intima-Media Thickness and Plaque Area Measurement in Ultrasound for Cardiovascular/Stroke Risk Monitoring.
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Baseline (10 days before the surgery), 30 days, 6 months and 12 months after the surgery
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cumulative incidence of adverse events during periprocedural period
Time Frame: Within 30 days after the surgery
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Incidence of death, major stroke, minor stroke, transient ischemic attack
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Within 30 days after the surgery
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Cumulative incidence of adverse events during postprocedural period
Time Frame: Between 30 days after the surgery and 12 months after surgery
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Incidence of death, major stroke, minor stroke, transient ischemic attack
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Between 30 days after the surgery and 12 months after surgery
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Change from baseline in lipid profile
Time Frame: Baseline (10 days before the surgery), 30 days, 6 months and 12 months after the surgery
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Total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol
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Baseline (10 days before the surgery), 30 days, 6 months and 12 months after the surgery
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Endocrine System Diseases
- Neoplasms by Site
- Neoplasms
- Autoimmune Diseases
- Immune System Diseases
- Eye Diseases
- Endocrine Gland Neoplasms
- Head and Neck Neoplasms
- Exophthalmos
- Orbital Diseases
- Goiter
- Thyroid Diseases
- Cardiovascular Diseases
- Graves Disease
- Hyperthyroidism
- Thyroid Neoplasms
- Euthyroid Goiter
Other Study ID Numbers
- 34C211
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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