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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03751605
Other study ID # PI2018_843_0047
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2018
Est. completion date February 1, 2023

Study information

Verified date February 2023
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The measurement of VO2 and VCO2 makes it possible to calculate the respiratory quotient (RQ) (VCO2 / VO2) which is a reflection of human energy metabolism and therefore of anaerobiosis. A study has been conducted in our department to demonstrate the ability of the indirectly measured respiratory quotient (RQ) from the inspired and exhaled breath analysis of the anesthetic respirator to predict the onset of anaerobic metabolism and postoperative complications in the operating room. Unipulmonary ventilation is the rule in thoracic surgery: it improves surgical exposure and protects the operated lung. However, no study has examined the impact of these mechanisms on the indirect measurement of RQ in unipulmonary ventilation. The main objective of our work is to validate indirect RQ measurement during unipulmonary ventilation. The secondary objective was to assess the predictability of postoperative complications of indirect QR.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date February 1, 2023
Est. primary completion date May 1, 2019
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age>18 years old - Adults admitted to the operating room for thoracic surgery requiring unipulmonary ventilation Exclusion Criteria: - Cardiac surgery - Laparoscopy - Preoperative oxygen therapy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
unipulmonary ventilation
observational study based on the computation of respiratory quotient in patient cohort treated by unipulmonary ventilation in routine thoracic surgery

Locations

Country Name City State
France CHU Amiens Amiens

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Indirect respiratory quotient during surgery
Secondary occurrence of at least one post-operative complication the aim is to predict the occurrence of at least one complication with the use of indirect respiratory quotient through study completion, an average of 6 months
See also
  Status Clinical Trial Phase
Withdrawn NCT03751579 - Indirect Measurement of Respiratory Quotient in Coelioscopic Surgery