Sympathetic Activity and Cardiometabolic Complications (NCT04495231) | Clinical Trial Compass
CompletedNot Applicable
Sympathetic Activity and Cardiometabolic Complications
Italy1,380 participantsStarted 2007-09-01
Plain-language summary
Recent studies on catecholamine physiology have shown a direct correlation with arterial hypertension, overcoming the exclusive role in the diagnosis and follow-up of chromaffin tumors.
Nevertheless, in literature, few studies explore and reveal the utility of testing metanephrines for the evaluation of sympathetic activity and its associated cardiometabolic complications in patients with essential hypertension.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Measurement of 24h urinary metanephrines at the laboratory of "City of Health and Science" hospital in Turin between 2007 and 2015
* Availability of contextual clinical patient data as collected in prospective registries of Piedmont region
Exclusion Criteria:
* Diagnosis of pheochromocytoma or paraganglioma (at the time of urinary metanephrines collection or within the following 5 years)
* Diagnosis of other forms of secondary hypertension
* Previous cardiovascular or cerebrovascular event
* Chronic heart failure
* eGFR \< 50 ml/min (according to CKD-EPI)
* Liver cirrhosis
* Acute conditions and/or hospitalization in ICU (at the time of urinary metanephrines collection)
* Assumption of acetaminophen during the day before the 24-hour urine collection
* Therapy with labetalol
* Therapy with sotalol
* Therapy with alpha-methyldopa
* Therapy with MAO inhibitors
* Therapy with tricyclic antidepressants
* Therapy with buspirone
* Therapy with phenoxybenzamine
* Therapy with sulfasalazine
* Therapy with L-Dopa
* Therapy with sympathomimetic drugs or other vasopressors
* Alcohol abuse
* Cocaine abuse
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.