Non-invasive Monitoring of Mixed Venous Oxygen Saturation Using the Capnodynamic Method in Adults

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFundación de Investigación Biomédica - Hospital Universitario de La Princesa

About this trial

The objective of this study is to compare the accuracy and correlation of the capnodynamic method for measuring mixed venous oxygen saturation (SvO2) with the standard reference method (pulmonary artery catheter), with the potential for the capnodynamic method to replace the traditional method in selected cases.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age > 18 years

Not participating in any other interventional study at the time of the study.

Patients under controlled mechanical ventilation in passive conditions.

Situations where the responsible physician deems that, for the benefit of clinical management and therapeutic decision-making, the patient would benefit from the placement of a pulmonary artery catheter (Swan-Ganz) and/or monitoring of central or mixed venous saturation.

Disqualifiers

Failure to obtain informed consent.

No need for invasive mechanical ventilation.

Trial population

The study will be conducted in the ICU of the Hospital Universitario de la Princesa. The study population will include all patients with medical conditions (respiratory or cardiac) who could benefit from the placement of a PAC and/or the monitoring of mixed venous saturation for clinical management and decision-making, or monitoring of central venous saturation if a pulmonary artery catheter is not required.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Mixed venous oxygen saturation (SvO2)

measured using the capnodynamic method in comparison with the invasive standard method using co-oximetry with a pulmonary artery catheter (PAC).

Time frame
24 hours

Secondary outcomes

1

Cardiac output

measured using the capnodynamic method in comparison with the invasive standard method using co-oximetry with a pulmonary artery catheter (PAC).

Time frame
24 hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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