Actively Recruiting

Age: 18Years +
All Genders
ID07211763

Comparison of Transcutaneous and Arterial Carbon Dioxide Monitoring During Jet Ventilation in Patients Undergoing Percutaneous Liver Tumour Radiofrequency Ablation

Led by Sahlgrenska University Hospital · Updated on 2025-10-08

100

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are comparing two methods of monitoring carbon dioxide levels during jet ventilation in patients undergoing percutaneous liver tumour radiofrequency ablation. Jet ventilation is used to reduce diaphragm movement during the procedure, improving conditions for the radiologist and reducing risk to surrounding tissue. Since standard end-tidal CO2 monitoring is not possible with jet ventilation, this study evaluates transcutaneous (through the skin) monitoring against arterial blood sampling to determine any differences between the two methods. Participants will receive the usual preoperative care and jet ventilation as per standard protocols. The study involves collecting data on carbon dioxide levels using both transcutaneous and arterial blood gas monitoring methods during the procedure. The data will be analyzed prospectively to assess discrepancies between the two monitoring techniques. Patients will contribute data during their routine care without any additional interventions. Researchers will measure the difference in carbon dioxide levels between the two methods during perioperative management. All patients will be monitored as usual, and the study will track data to analyze the accuracy and reliability of each monitoring method. Participation involves no change to standard treatment and will last only for the duration of the procedure and immediate perioperative period.

CONDITIONS

Brief Title

Comparison of Transcutaneous and Arterial Carbon Dioxide Sampling During Jet Ventilation, a Prospective. Study on Patients Undergoing Percutaneous Liver Tumour Radiofrequency Ablation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients undergoing percutaneous radiofrequency liver tumour ablation requiring jet ventilation
Not Eligible

You will not qualify if you...

  • Any disease or condition that is not compatible with jet ventilation

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - Perioperative period

Participants undergoing percutaneous liver tumour radiofrequency ablation with jet ventilation have transcutaneous and arterial carbon dioxide levels monitored during the procedure.

1 procedure visit (in-person)

Trial Site Locations

Total: 1 location

1

Sahlgrenska University Hospital

Gothenburg, Sweden

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Research Team

F

Fredrik Olsen, MD PhD

C

Carl Hallgren, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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