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Non Invasive Cardiac Output Evaluation With Starling SV for Lung Elective Surgery

Non Invasive Cardiac Output Evaluation With Starling SV for Lung Elective Surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04251637
Acronym
NICOLE
Enrollment
51
Registered
2020-02-05
Start date
2020-09-25
Completion date
2021-03-13
Last updated
2021-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Surgery, Thoracic

Keywords

esophageal Doppler, thoracic surgery, pulmonary exeresis

Brief summary

Intraoperative hemodynamic optimization decreases postoperative complications and length of stay in high risk patient. Therefore, continuous monitoring of cardiac output (Qc) is recommended to guide fluid management. Thoracic bio-reactance is a recent technique that allows cardiac output non-invasive monitoring. However, additional clinical validation studies in humans are required to better define the typologies of patients for whom this monitoring could be proposed routinely. Lung surgery is defined as an intermediate or high risk surgery regarding postoperative cardiac complications. However, surgical patients rarely benefit from continuous monitoring of cardiac output, the available methods being considered too invasive or insufficiently reliable in daily practice. Thoracic bio-reactance (Non Invasive Cardiac Output Monitor (NICOM) Starling SV) has not been studied in this subgroup of clinically relevant patients.

Interventions

OTHERCardiac output monitoring with Starling SV.

Intraoperative monitoring of cardiac output by esophageal Doppler, NICOM Starling SV and collection of values for each patient at at least 7 predefined intraoperative times.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients * Scheduled in Louis Pradel hospital operating theater (Lyon University Hospital) for elective Lung surgery (lobectomy, bilobectomy or pneumonectomy); by thoracotomy and / or thoracoscopy. * Having stated their non opposition to be part of this protocol

Exclusion criteria

* Pregnant women ; * unemancipated minors; * Persons unable to express their consent; * Patients with contraindications to the placement of an oesophageal Doppler probe * Patients with suspicion of pathology or oesogastric lesion (dysphagia, diverticulum, stenosis ...) * Patients known for stage 2 or higher oesophageal varices * Patients with a history of significant mediastinal irradiation, or bariatric surgery. * Patients who have been treated in a therapeutic trial within 30 days of enrollment or who wish to participate in an ongoing study that may interfere with this study. * Persons benefiting from legal protection measures; * Patients unable to understand study objectives or refusing to comply with postoperative instructions

Design outcomes

Primary

MeasureTime frameDescription
cardia output measurementDay 0The primary endpoint is the accuracy of the cardiac output value measured with the NICOM Starling SV vs. oesophageal Doppler in thoracic controlled pulmonary exeresis surgery in adults. The accuracy considered valid and reliable will be defined as the error percentage for the Cardiac Output (CO) with an acceptability (concordance) threshold of 30 %. The accuracy will be evaluated on the totality of the time points of interrest. All data will be recorded at several time points interest (T0-T7) during surgery: * T0 Post Induction / supine position * T1 Lateral position closed Thorax / bipulmonary ventilation * T2 Lateral position closed Thorax / selective unipulmonary ventilation. * T3 Lateral position open Thorax * T4 pleural cavity being Washed * T5 Before Lung Recruitment Maneuver * T6 During Positive End Expiratory Pressure (PEEP) Standardized Pulmonary Recruitment Maneuver 30 cmH20 30 seconds * T7 End of Surgery / Awakening in lateral decubitus

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026