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Status unknownNCT05411250Updated Jun 9, 2022

Early Diagnosis of Therapy-associated Cardiotoxicity Basing on PET/CT in Lymphoma

An observational study in Positron-Emission Tomography, sponsored by Peking University Cancer Hospital & Institute. Status unknown. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-06-09.

Sponsored by Peking University Cancer Hospital & Institute · Observational

The sponsor has not verified this record recently (last verified Jun 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
40
Ages
18 Years to 75 Years
Sex
All
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Study summary

To explore the value of 18F-fluorodeoxyglucose (FDG) PET/CT imaging in early diagnosis of treatment-related cardiotoxicity (TACT) of lymphoma using visual method and semi-quantitative method.

Read the detailed description

First of all, the cardiac 18F-FDG uptake in patients with lymphoma will be observed by visual method: according to the uptake site, it will be divided into left ventricular uptake and biventricular uptake, and according to the degree of uptake, it will be divided into equal uptake (myocardial uptake is lower than cardiac blood pool uptake), moderate uptake (myocardial uptake is between cardiac blood pool uptake and liver uptake) and high uptake (myocardial uptake is higher than liver uptake). According to the uptake pattern, it can be divided into diffuse and segmental uptake.Then,using the region of interest method to mesure the value of myocardial uptake of 18F-FDG.The difference value of heart's SUVmax (Δ SUVmax- heart) and% Δ SUVmax- heart before and after chemotherapy or immunotherapy will be calculated. And SUVmax- heart / SUVmax- mediastinum ratio, SUVmax- heart / SUVmax- liver ratio and SUVmax- heart / SUVmax- background ratio (left gluteal muscle) after treatment. Taking the abnormality of ECG (early TACT) as the end point.

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Conditions studied

  • Positron-Emission Tomography

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Keywords

  • cardiotoxicity
  • early
03

In context

Cardiotoxicity

264 studies on the registry are indexed under Cardiotoxicity; 71 are open to participants now.

This study's planned enrollment of 40 is below the median of 100 across 125 observational studies indexed under Cardiotoxicity.

Browse Cardiotoxicity studies →

Lead sponsor

Peking University Cancer Hospital & Institute is the lead sponsor of 261 studies on the registry; 128 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Patients with malignant tumor after chemotherapy or immunotherapy

Inclusion criteria

  1. No previous history of heart disease.
  2. normal echocardiography, ECG and laboratory tests (creatine kinase, myoglobin, troponin, brain natriuretic peptide) before treatment.

3.18F-FDG PET/CT examination before and after treatment

Exclusion criteria

-

Exclusion Criteria:

1.receiving radiotherapy and chemotherapy at the same time. 2.previous chest radiotherapy. 3. with severe hepatic or renal dysfunction.

-

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
40 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. SUVmax

    the standardized uptake value

    Time frame: 150 days

Secondary outcomes

  1. SUVR

    the ratio of the standardized uptake value for the heart to the normal tissue such as hepatic blood poor and gluteus

    Time frame: 150 days

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 9, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05411250
Lead sponsor
Peking University Cancer Hospital & Institute
Responsible party
Xuejuan Wang,MD (Principal INvestigaor, Peking University Cancer Hospital & Institute) — Principal investigator
First posted
Jun 9, 2022
Start date
Jun 1, 2022 (estimated)
Primary completion
May 31, 2023 (estimated)
Completion
Jul 31, 2023 (estimated)
Last update
Jun 9, 2022

Study contacts

Xuejuan Wang, MD
Contact
xuejuan_wang@hotmail.com
8601088196363
Zhi Yang, PhD
study director · Peking cancer hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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