Trial Outcomes & Findings for Preoperative Pocket Echocardiography Trial (NCT NCT02589808)
NCT ID: NCT02589808
Last Updated: 2019-10-23
Results Overview
Number of participants who had the same results with both diagnostic device (GE VScan and full transthoracic echocardiogram)
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
76 participants
Primary outcome timeframe
30min
Results posted on
2019-10-23
Participant Flow
Participant milestones
| Measure |
All Participant
All Participant went through on full transthoracic echocardiography then GeVscan
|
|---|---|
|
Overall Study
STARTED
|
76
|
|
Overall Study
COMPLETED
|
76
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Race and Ethnicity were not collected from any participant.
Baseline characteristics by cohort
| Measure |
Echocardiography
n=76 Participants
Cardiac ultrasound scan.
Echocardiography: Pocket ultrasound device.
|
|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=76 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
40 Participants
n=76 Participants
|
|
Age, Categorical
>=65 years
|
36 Participants
n=76 Participants
|
|
Sex: Female, Male
Female
|
56 Participants
n=76 Participants
|
|
Sex: Female, Male
Male
|
20 Participants
n=76 Participants
|
|
Region of Enrollment
United Kingdom
|
76 participants
n=76 Participants
|
PRIMARY outcome
Timeframe: 30minNumber of participants who had the same results with both diagnostic device (GE VScan and full transthoracic echocardiogram)
Outcome measures
| Measure |
Echocardiograph
n=76 Participants
Fully accredited echocardiography laboratory
|
|---|---|
|
Number of Participants With Same Results With GE VScan and Full Transthoracic Echocardiogram
|
66 Participants
|
Adverse Events
Echocardiography
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place