ClinicalTrials.gg
RecruitingNCT06327425Updated Aug 21, 2024

MCG for Localization of Tachyarrhythmia's Origin

An interventional study of Magnetocardiography in Tachyarrhythmia, Atrial Flutter and Paroxysmal Supraventricular Tachycardia, sponsored by Qilu Hospital of Shandong University. Recruiting at 1 site in China. Open to participants aged 18 Years to 79 Years. Per ClinicalTrials.gov, last updated 2024-08-21.

Primary conditionTachycardia, VentricularRegistry: TachycardiaReclassifiedWhy we changed it
Registry
Tachycardia — the first condition term the registry derived for this study.
ClinicalTrials.gg
Tachycardia, Ventricular
Why
  1. The study's listed conditions name Tachycardia, Ventricular, a narrower term within Tachycardia.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Qilu Hospital of Shandong University · Not applicable, Interventional, and Diagnostic

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 11 months ago, but the record still lists the study as recruiting.
  • Started Mar 2024; still recruiting 2 years 7 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
1,000
Allocation
Non-randomized
Ages
18 Years to 79 Years
Sex
All
01

Study summary

This is an exploratory research aiming to accurately identify the site of origin of tachyarrhythmia using Magnetocardiography (MCG), which will have guiding significance for early diagnosis, the formulation of treatment plans and preoperative positioning for radiofrequency ablation.

02

Conditions studied

  • Tachyarrhythmia
  • Atrial Flutter
  • Paroxysmal Supraventricular Tachycardia
  • Atrial Tachycardia
  • Atrial Fibrillation
  • Premature Ventricular Contraction
03

In context

Tachycardia, Ventricular Reclassified

451 studies on the registry are indexed under Tachycardia, Ventricular; 120 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 71 across 280 interventional studies indexed under Tachycardia, Ventricular.

Browse Tachycardia, Ventricular studies →

Lead sponsor

Qilu Hospital of Shandong University is the lead sponsor of 310 studies on the registry; 188 are open to participants now.

Compared within Tachycardia, Ventricular, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Tachycardia. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 79 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18-79 years old;
  • Those whose conditions are comparatively stable and who have been diagnosed by an attending physician (or physicians with higher qualifications) with paroxysmal supraventricular tachycardia, atrial tachycardia, atrial flutter, atrial fibrillation, or premature ventricular contractions, and who are capable of performing MCG and cardiac electrophysiologic examinations after evaluation.
  • Signed .

Exclusion criteria

Exclusion Criteria:

  • Those with known structural heart disease such as cardiomyopathy and valvular disease;
  • Those with history of other cardiovascular diseases such as pulmonary embolism and aortic dissection;
  • Those with connective tissue diseases (lupus erythematosus, rheumatoid arthritis, dermatomyositis, polyarteritis nodosa, etc.) combined with cardiac complications;
  • Those with obvious abnormal thyroid function, severe anemia or other blood diseases and other diseases that obviously affect the circulating blood supply;
  • Those with Obese (>30kg/cm2) or underweight (BMI\<18kg/cm2);
  • Those with malignant tumors;
  • Professional athletes, pregnant or breastfeeding women, alcoholics;
  • Those with acute diseases or critical illnesses in other systems, such as acute or severe respiratory diseases, abnormal liver function or renal function, etc.;
  • Those with infectious diseases or communicable diseases;
  • Those who are unable or fail to perform magnetocardiography due to claustrophobia, physical impairment, etc.;
  • Unable to or fail to cooperate with the corresponding research requirements.
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,000 participants (estimated)

Study arms

  • Experimental
    Patients with atrial tachycardia

    Patients with atrial tachycardia will receive dynamic ECG, MCG and cardiac electrophysiologic examinations.

    Device: Magnetocardiography

  • Experimental
    Patients with atrial flutter

    Patients with atrial flutter will receive dynamic ECG, MCG and cardiac electrophysiologic examinations.

    Device: Magnetocardiography

Interventions

  • DeviceMagnetocardiography

    Magnetocardiography

06

What researchers measure

Primary outcomes

  1. Efficacy of MCG to detect the site of origin of Tachyarrhythmia using cardiac electrophysiology as a reference standard.

    Sensitivity, specificity, and area under the ROC curve are performed for assessing the efficacy.

    Time frame: 12 month course of the disease

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 21, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06327425
Responsible party
Sponsor
First posted
Mar 25, 2024
Start date
Mar 14, 2024
Primary completion
Dec 2024 (estimated)
Completion
Feb 2025 (estimated)
Last update
Aug 21, 2024

Study contacts

Jiaojiao Pang, Doctor
Contact
jiaojiaopang@126.com
0086-0531-82165398
Yuguo Chen, Professor
principal investigator · Qliu Hospital of Shandong University

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion