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Cardiovascular Disease OtherCV-UNEXPET/TCNCT06774391

CARDIOVASCular Unexpected fiNdings in patiEnts Undergoing eXecution of PET/tc

An observational study of Cardiovascular Disease Other, run by IRCCS Azienda Ospedaliero-Universitaria di Bologna at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this single-center observational study is to retrospectively evaluate incidental findings at the cardiovascular level in a selection of patients referred to the O.U. of Nuclear Medicine of Policlinco S.Orsola-Malpighi who underwent a PET/CT investigation. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Cardiovascular Disease Other
How many people
1,000 participants
Where
1 siteItaly
Study dates
1 Jan 2017to 31 Dec 2020
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients who performed PET/CT examinations at the Sant'Orsola-Malpighi Nuclear Medicine OU in the period between 01/01/2017 and 31/12/2019. Based on the services provided, it is estimated about 35,000-45,000 total examinations. Of these, through the infortmatic approach described just above, only patients of interest will be selected: an estimated 1,000. It should be noted that in the event that each patient has performed more than one PET/CT scan for the purpose of the study, a different patient ID will be identified for each investigation performed.

Who may be able to join

  • All patients referred to the U.O. of Nuclear Medicine of Policlinico S.Orsola-Malpighi who underwent a PET/CT investigation from 01/01/2017 to 31/12/2019.
  • age > 18 years old

Who cannot join

  • Pregnant women

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • IRCCS - Azienda Ospedaliero-Universitaria di Bologna

    Bologna, 40138

Other trials in Italy

About this study

Official title: CARDIOVASCular Unexpected fiNdings in patiEnts Undergoing eXecution of PET/tc (CV-UNEXPET/TC)

The goal of this single-center observational study is to retrospectively evaluate incidental findings at the cardiovascular level in a selection of patients referred to the O.U. of Nuclear Medicine of Policlinco S.Orsola-Malpighi who underwent a PET/CT investigation.

In particular, the present study is aimed to explore in such patients occasional findings of hypercapturing radiopharmaceutical findings specifically referred to:

Read more
  • infection inflammatory processes of implantable cardiac devices (ICDs, pacemakers);
  • phenomena affecting the atria during episodes of atrial fibrillation;
  • infection and inflammatory processes of cardiovascular structures (endocarditis, myocarditis, pericarditis, amyloidosis).

Patients who performed PET/CT examination at the Sant'Orsola-Malpighi Nuclear Medicine O.U. during the period between 01/01/2017 and 31/12/2019 will be included in this registry. Any cardiovascular events that occurred within the Sant'Orsola-Malpighi Polyclinic setting and up to 3 months after the date of the PET/CT scan will be subsequently evaluated.

Read the detailed description

The present study aims to investigate the role of PET/CT investigation in the detection of abnormal ancillary findings, in this case of the cardiovascular type. This aspect, at first glance of secondary importance with respect to the reasons why a patient undergoes this diagnostic examination, is actually of some importance, since early detection of some significant incidental findings (otherwise misrecognized because they are not related to any symptomatic cortex) can often negatively influence several patient-related factors:

  • Response to therapy (e.g., chemotherapy);
  • Comorbidities;
  • Life expectancy;
  • Quality of life.

All data of patients referred to the U.O. of Nuclear Medicine of Policlinico S.Orsola-Malpighi who underwent a PET/CT investigation from 01/01/2017 to 31/12/2019 will be collected. Of these patients, the biographical data, clinical news, biochemical tests, any other imaging investigations (CT, echocardiography, MRI) will be collected. Within the population, patients who, upon review and anonymization of PET/CT images, show significant radiotracer hyperfixation at the cardiovascular level will be identified. Incidental findings referable to:

  • infection and inflammatory phenomena of implantable cardiac devices (ICDs, pacemakers);
  • misdiagnosed episodes of atrial fibrillation;
  • infection and phlogistic phenomena of cardiovascular structures (endocarditis, myocarditis, pericarditis, amyloidosis).

The computerized approach of the study involves the following steps. Starting from the computerized database that collects the main clinical-anamnestic information of all patients afferent to the Nuclear Medicine Cluster of Policlinico S.Orsola-Malpighi (ASTRIM), specific queries will be created for automatic filtering by keywords of only the patients of interest, specifically:

  • For patients who carry intracardiac devices, selection will be by keywords such as "pacemaker," "defibrillators," "ICD"; "CIED."
  • For patients with a history of amyloidosis or heart failure, selection is through keywords such as "amyloidosis" "heart failure."
  • For patients with a history of atrial fibrillation, selection is through keywords such as "atrial fibrillation," "AF."

This initial search will be complemented by a second selection of patients whose PET/CT report contains keywords that may point to the presence of hypermetabolic findings at the cardiac level. By entering keywords such as "pacemaker," "device," "electrocatheter," "atrial," "atrial fibrillation," and "amyloidosis" on the ERIS computer system, it will be possible to quickly identify all patients with suspicious findings at the cardiac level and reported by the nuclear physician on the validated report. In addition, the names of patients with intracardiac devices followed up at the Cardio-Thoracic-Vascular Pole of Policlinico S.Orsola-Malpighi will be provided; of them, it will be possible to extrapolate those who underwent PET/CT during the period taken into consideration of the study. Therefore, it is estimated that from a total database of approximately 35,000-40,000 examinations, about a thousand patients will be selected through the procedures described above. From the excluded patients with sufficient recorded clinical data, control groups matched for age, sex, and indication for evaluation by PET/CT will be produced.

Therefore, an initial analysis will be conducted in describing the selected group of patients with cardiovascular-type findings, analyzing the uptake patterns and semi-quantitative parameters (Standardized Uptake Value, SUV) and comparing them with the control group.

Then we will conduct through computerized data from three company databases (ERIS, Online Medical Records and the Cardio-Thoracic-Vascular Pole Implantable Cardiac Device Carriers Registry), a maximum 3-month monitoring aimed at identifying any hospital admissions for cardiovascular reasons justified by the previously found PET/CT finding.

The following data will be evaluated for each patient:

  • Current medical history/concurrent therapies
  • Past concomitant therapies
  • Laboratory tests
  • Inclusion/exclusion criteria
  • PET/CT examination. In the 3 months following the PET/CT investigation, any cardiovascular events occurring in that time window and recorded within the S.Orsola-Malpighi Polyclinic will be evaluated.

The study is observational, noninterventional in nature. Patients were treated according to clinical practice in accordance with the physician's judgment and the information in the Technical Data Sheet of each individual Radiopharmaceutical.

Descriptive analysis will be conducted using appropriate statistics: Student's t-test, chi-square test. Significance will be achieved with p-values<0.05. Data will be presented for the population considering all patients included in the study.

The objective of the study is to search for incidental findings in an unselected population of patients who have undergone a PET/CT investigation. The estimated sample size will be about 1,000 patients, drawn from a total database that should include the totality of PET/CT investigations performed at the O.U. of Nuclear Medicine in Bologna and is estimated at about 35,000-45,000 examinations.

Keywords
CIED, amyloidosis, cardiomyopathies, atrial fibrillation, PET/TC
Medical subject headings
Amyloidosis, Cardiomyopathies, Atrial Fibrillation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prevalence of all incidental cardiovascular findings hypercapturing 18-fluorodeoxyglucose and not justified by history

    The primary objective of the study is to assess the prevalence of all incidental cardiovascular findings hypercapturing the radiopharmaceutical and not justified by history, with subsequent characterization of the sites in relation to the indication for performing PET-CT.

    Measured: At enrollment

Secondary outcomes (1)
  1. incidence of hospitalization for cardiovascular causes in subjects with incidental findings hypercapturing the radiopharmaceutical, compared with subjects without such findings compared with negative subjects

    The secondary objective of the study is to evaluate the incidence of hospitalization for cardiovascular causes in subjects with incidental findings hypercapturing 18-FDG, compared with subjects without such findings compared with negative subjects. The analysis will be limited to patients followed at Policlinico S. Orsola Malpighi for a period of not less than 3 months after the PET/CT scan was performed, or who presented with a cardiovascular event within that time window.

    Measured: From enrollment to 3 months after

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Jan 2025
  2. Study start1 Jan 2017
  3. Primary completion31 Dec 2019
  4. Study completion31 Dec 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
1,000 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06774391
Sponsor's protocol ID
CV-UNEXPET/TC
Acronym
CV-UNEXPET/TC
Status last verified
Nov 2024
First submitted
9 Jan 2025
Last updated
14 Jan 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cardiovascular Disease Other, run by IRCCS Azienda Ospedaliero-Universitaria di Bologna at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prevalence of all incidental cardiovascular findings hypercapturing 18-fluorodeoxyglucose and not justified by history (time frame: At enrollment). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jan 2025.

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