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Impact of the ProbeFix on the Workflow of Pharmacological Stress Echocardiography Examinations

A

Amir Abbas Mahabadi

Status

Withdrawn

Conditions

Coronary Artery Disease

Treatments

Other: ProbeFix
Other: Manual hold

Study type

Interventional

Funder types

Other

Identifiers

NCT04016363
19-TEMP815870-BO

Details and patient eligibility

About

Pharmacological stress-echocardiography examinations are routinely performed in daily clinical practice. Usually, the echo probe is manually placed on the patient's thorax by the physician. The ProbeFix is a novel device, enabling the fixation of the ultrasound probe on the patient's thorax. Therefore, there is no need to manually hold the probe. This may improve the standardization of the examination and my reduce its duration. The present trial will investigate, whether the utilization of the ProbeFix reduces the duration of stress-echocardiography examinations and improves standardization of image acquisition.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing clinically indicated pharmacological stress-echocardiography
  • Willingness to participate

Exclusion criteria

  • Pharmacological stress echocardiography indication other than evaluation of stress induced ischemia (e.g. Low-Flow-Low-Gradient aortic valve stenoseis)
  • poor image quality
  • Early termination of the stress-echocardiography examination for clinical reasons

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

ProbeFix arm
Experimental group
Description:
The echocardiography probe is fixated on the patient's thorax using the ProbeFix
Treatment:
Other: ProbeFix
Controll arm
Active Comparator group
Description:
The sonographer manually holds the probe on the patient's thorax
Treatment:
Other: Manual hold

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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