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Comparative Analysis of CO2 Monitoring Methods in Patients With CF Undergoing General Anesthesia

Nationwide Children's Hospital logo

Nationwide Children's Hospital

Status

Completed

Conditions

Cystic Fibrosis

Treatments

Diagnostic Test: Capillary CO2 (CapCO2)
Other: End tidal CO2 (EtCO2)
Diagnostic Test: Arterial blood gas (ABG)
Device: Transcutaneous CO2 (TCO2)

Study type

Interventional

Funder types

Other

Identifiers

NCT03734822
IRB15-00797

Details and patient eligibility

About

Four methods are routinely used to monitor CO2 in patients. End tidal CO2 (EtCO2) is monitored through the endotracheal tube during general anesthesia. CO2 is also monitored in other healthcare settings transcutaneously (TCO2), via finger stick capillary CO2 (CapCO2), and arterial blood gas (ABG). The purpose of this study is to perform all four measurements simultaneously during general anesthesia to identify which measure provides the most accurate data with the least amount of patient risk.

Enrollment

47 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Have a confirmed diagnosis of cystic fibrosis (positive sweat chloride value ≥ 60 mEq/L) and/or genotype with two identifiable mutations consistent with CF, accompanied by one or more clinical features consistent with the CF phenotype)
  • Hemodynamically stable undergoing general anesthesia for a scheduled procedure

Exclusion criteria

  • Patients not diagnosed with CF
  • CF patients undergoing anesthesia for emergency procedures

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

47 participants in 1 patient group

CF
Other group
Description:
Cystic fibrosis patients undergoing general anesthesia.
Treatment:
Diagnostic Test: Capillary CO2 (CapCO2)
Device: Transcutaneous CO2 (TCO2)
Other: End tidal CO2 (EtCO2)
Diagnostic Test: Arterial blood gas (ABG)

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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