N/A N=76 Diagnostic

Preoperative Pocket Echocardiography Trial

Preoperative Period · Echocardiography

Bottom Line

View on ClinicalTrials.gov: NCT02589808 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Oct 2019

Primary outcome: Primary: Number of Participants With Same Results With GE VScan and Full Transthoracic Echocardiogram — 66 Participants — p=0.0005

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Full TTE (Device); GE Vscan (Device)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Imperial College London
Primary completion: Feb 2016

Outcome Measures

Outcome	Result	p-value
PRIMARY Number of Participants With Same Results With GE VScan and Full Transthoracic Echocardiogram	66	0.0005 sig

Summary

This study will compare findings using a handheld ultrasound device (GE VScan) with those using a diagnostic ultrasound machine in adult patients referred for transthoracic echo (TTE), prior to non-cardiac surgery at Hammersmith Hospital, London. The handheld TTE (VTTE) will follow the standard Hammersmith Hospital diagnostic TTE (DTTE) protocol (with the exception of spectral Doppler) and will be reported on a simple 'tick box' form. A different echocardiographer will then perform and report the DTTE as per routine practice. The results from VTTE and DTTE will be directly compared. The echocardiographers performing the VTTE and DTTE are all fully accredited in diagnostic TTE and will be blinded to each others findings. The study aims to recruit a total of 96 patients with an anticipated study completion date of November 2015.

Eligibility Criteria

Inclusion Criteria

Adult surgical (non-cardiac) patients referred preoperatively for resting transthoracic echocardiogram

Exclusion Criteria

No consent or withdrawal of consent.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02589808). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.