CClinicalTrials.gg
RecruitingNCT05623969Updated Nov 30, 2022

Markers of Atrial Cardiopathay

An observational study in Atrial Cardiopathy, sponsored by Assiut University. Recruiting at 1 site in Egypt. Open to participants aged 17 Years to 90 Years. Per ClinicalTrials.gov, last updated 2022-11-30.

Sponsored by Assiut University · Observational

From the registry’s dates

  • Primary completion was expected by Nov 2025, 11 months ago, but the record still lists the study as recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
17 Years to 90 Years
Sex
All
01

Study summary

Marker of atrial cardiopathay as apredictor value of ischemic stroke

Read the detailed description

detection of the presence of atrial dysfunction or atrial cardiopathy and its degree among patients complaining of palpitation, with a one-year follow-up for any cardioembolic events (stroke /TIA).

02

Conditions studied

  • Atrial Cardiopathy

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03

In context

Heart Diseases

3,639 studies on the registry are indexed under Heart Diseases; 461 are open to participants now.

This study's planned enrollment of 30 is below the median of 294 across 1,241 observational studies indexed under Heart Diseases.

Browse Heart Diseases studies →

Lead sponsor

Assiut University is the lead sponsor of 4,901 studies on the registry; 2,098 are open to participants now.

Of its 13 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
17 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

  • Patients complaining of palpitation referred for Holter monitoring

Inclusion criteria

  • Patients complaining of palpitation referred for Holter monitoring

Exclusion criteria

Exclusion Criteria:

    • Valvular AF, moderate to severe mitral/ tricuspid/ aortic stenosis or regurgitation.

      • Recent myocardial infarction within 3 months.
      • Acute pulmonary embolism.
      • Newly onset AF during or shortly after cardiac surgery.
      • Specific type of cardiomyopathy such as cardiac amyloidosis, obstructive hypertrophic cardiomyopathy.

Decompensation stage of organ failure

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testHolter ,Echo , Speckle tracking echocardiography

    A 24-h ambulatory Holter Echocardiography Speckle tracking echocardiography (STE)

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What researchers measure

Primary outcomes

  1. Detection of any underlying arrythmia after holter monitoring for twenty four hours

    Detection of any underlying arrythmia after holter monitoring for twenty four hours

    Time frame: Detection of any underlying arrythmia after holter monitoring for twenty four hours

Secondary outcomes

  1. Detection of atrial dysfunction or atrial cardiopathy and its degree among patients complaining of palpitation, with 6 month follow-up for any cardioembolic events (stroke /TIA).

    Detection of atrial dysfunction or atrial cardiopathy and its degree among patients complaining of palpitation, with 6 month follow-up for any cardioembolic events (stroke /TIA).

    Time frame: Detection of atrial dysfunction or atrial cardiopathy and its degree among patients complaining of palpitation, with 6 month follow-up for any cardioembolic events (stroke /TIA).

07

Study locations

1 of 1 sites recruiting
  • Mariam zarief farhan
    Assiut, 23123, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

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 Nov 30, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05623969
Lead sponsor
Assiut University
Responsible party
Mariam Zarief Farhan (principal investigator, Assiut University) — Principal investigator
First posted
Nov 21, 2022
Start date
Nov 30, 2022 (estimated)
Primary completion
Nov 1, 2025 (estimated)
Completion
Nov 1, 2025 (estimated)
Last update
Nov 30, 2022

Study contacts

Mariam zarief farhan, resident
Contact
mariamzarif134@gmail.com
01009427245
Amr Ahmed Aly Youssef, professor
Contact
amryoussef111@aun_edu.eg
01027355511
Mohammed Aboelkassem Farghal, professor
principal investigator · Assiut University

Oversight

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

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