NCT06962748

Brief Summary

Cardiac output (CO) is challenging to measure at the bedside. The traditional gold standard for measuring CO requires the insertion of a pulmonary artery catheter which is invasive, associated with a risk for serious complications \[3\],with no clinical benefits. The cerebral blood flow (CBF) is considered to be a proportion of total cardiac output (CO). It has been stated earlier that approximately 15% of resting CO is distributed to the brain. Therefore, the flow through the CCA might serve as a surrogate parameter for CO.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
105

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 30, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

May 8, 2025

Completed
24 days until next milestone

Study Start

First participant enrolled

June 1, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

March 12, 2026

Status Verified

April 1, 2025

Enrollment Period

6 months

First QC Date

April 30, 2025

Last Update Submit

March 10, 2026

Conditions

Keywords

ETCO2- Cardiac output-Carotid blood flow

Outcome Measures

Primary Outcomes (1)

  • correlation of ETCO2

    we assume that the change in the gradient of carbon dioxide release over a time in mechanically ventilated patients may be directly proportionate to the cardiac output and could reflect it. In the current study we will correlate the aforementioned hypothesis with the change in the cardiac output compared to the change in the carotid blood flow as revealed by the change in the cardiac output as measured by the transthoracic echocardiography.

    during operation

Study Arms (3)

ETCO2

ACTIVE COMPARATOR

The patients EtCO2 will be recorded and the average of the reading over a time interval of 30 minutes will be recorded and correlated to the cardiac output as measured by both the carotid blood flow and the TTE

Diagnostic Test: ETCO2

TTE CO

ACTIVE COMPARATOR

a transthoracic echocardiography will be done to measure the cardiac output

Diagnostic Test: TTE CO measurment

carotid blood flow

ACTIVE COMPARATOR

The patients' Cardiac output as measured before will be correlated with the carotid blood flow after scanning the carotid artery to exclude a significant lesion as measured by the following equation and the average of a three consecutive reading will be recorded

Diagnostic Test: cerebral blood flow measurment

Interventions

measuring CO using cerebral blood flow

carotid blood flow
TTE CO measurmentDIAGNOSTIC_TEST

measuring CO using TTE

TTE CO
ETCO2DIAGNOSTIC_TEST

measure the average ETCO2 over 30 minutes period

ETCO2

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • The patients age will be ranged from 18-55 years,
  • ASA physical status I-II,
  • General surgeries not involving the head and neck
  • Orthopedic surgeries involving the lower limb
  • Patients in supine posture

You may not qualify if:

  • Those with Respiratory disease including but not limited to Pneumonia, COPD, Restrictive lung disease and ARDS
  • Those with anemia.
  • Patients' refusal to participate in the study.
  • Thoracic surgeries.
  • Morbidly obese patients.
  • Significant carotid artery disease.
  • Surgeries of less than 2-hour duration.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ain Shams University

Cairo, Abbasiya, 12245, Egypt

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

April 30, 2025

First Posted

May 8, 2025

Study Start

June 1, 2025

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

March 12, 2026

Record last verified: 2025-04

Locations