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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04114474
Other study ID # transthoracic echocardiograpy
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2017
Est. completion date December 30, 2018

Study information

Verified date October 2019
Source South Egypt Cancer Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The extent focused transthoracic echocardiography when done pre-operatively to patients admitted for elective surgery and suspected to be at risk of cardiac disease specially the geriatric population can affect perioperative anesthetic management of these patients.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date December 30, 2018
Est. primary completion date December 1, 2018
Accepts healthy volunteers No
Gender All
Age group 60 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients above 60 years of age ASAI and ASA II were included

Exclusion Criteria:

- history of cardiac disease, history of previous postoperative cardiac complications and symptoms or signs of cardiac diseases.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
TRANSTHORACIC ECHOCARDIOGRAPY
TTE (Vivid I echocardiography machine General Electric Healthcare, Milwaukee, WI, USA) with a 3S-RS (1.5-3.6 MHz) transthoracic probe). was done by professional anesthesiologist following the :Hemodynamic Echocardiography Assessment in Real Time ( HEART) protocol. According to the clinical findings of TTE patients may be either free or have one or more of the following haemodynamic states normal, empty, vasodilated ,left ventricular systolic or diastolic failure, left ventricular systolic and diastolic failure, and right ventricular failure, valve stenosis or regurgitation of at least moderate severity

Locations

Country Name City State
Egypt South Egypt Cancer Institute, Assiut University, Arab Republic of Egypt Assiut

Sponsors (1)

Lead Sponsor Collaborator
South Egypt Cancer Institute

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lt. Ventricular EDV Transthoracic echocardiography (TEE) LVEDV Change from Baseline pre operative LVEDV to first day postoperative
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