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NCT00954733 · ClinicalTrials.gov registry record · NA

A Comparison of the Detection of Hypoventilation During Deep Sedation Utilizing Nasal End Title CO@ Versus Transcutaneous CO2 Measurement Techniques

A NA study, sponsored by Northwestern University.

Completed
Registry status
NA
Development phase
40
Enrollment target

NCT00954733: Completed NA study, sponsored by Northwestern University.

NCT00954733 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00954733, a NA study, has completed, sponsored by Northwestern University.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

The estimation of the partial pressure of carbon dioxide (PCO2) in the arterial blood is used to judge the adequacy of ventilation during spontaneous and controlled ventilation. Although the gold standard for monitoring PCO2 remains arterial blood gas sampling, this requires an invasive procedure and provides only an intermittent estimate of what is frequently a continuously changing value. The solution to this problem has been the development and validation of accurate noninvasive monitoring techniques which provide a continuous intraoperative estimate of PCO2.The most commonly used noninvasive technique to monitor PCO2 is measurement of the end tidal CO2 (PECO2) . However, sampling errors and patient -related issues such as ventilation-perfusion mismatch, patient positioning or decreases in pulmonary blood flow may influence the accuracy of PECO2 monitoring (1-3). Nasal capnography has been proved to be an accurate monitor during the post-operative period (4) but its ability to accurately detect hypoventilation associated with deep sedation has not been studied. According to the American Society of Anesthesiologist standards for basic monitoring, continuous capnography is required for all patients undergoing general anesthesia but it is optional for MAC/sedation cases. The need for CO2 monitoring has been studied by other medical specialties that use procedural sedation, including gastroenterology (12) and emergency medicine (13, 14) and many specialties now recommend capnography as a standard monitor. Patients receiving supplemental oxygen may experience significant persistent hypoventilation leading to progressive hypercarbia and acidosis which may go undetected for a significant time interval since the routinely monitored SpO2 may be maintained within normal range. A recent study has shown that despite the fact that end tidal CO2 is reliable in detecting apnea , increasing oxygen flow rates decrease the amplitude of measured CO2, probably via dilution, making

Primary Outcome

Evaluate the correlation between PaCO2- TcCO2 in detecting hypoventilation for patients undergoing deep sedation Absolute mean difference between TcCo2 and the PA Co2

Interventions

  • OTHER Arterial blood draw

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2009-06
Est. Completion 2009-08
Phase NA
Northwestern University

1,209 total trials

What the finished NCT00954733 record still lists

NCT00954733 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Arterial blood draw is the first listed.

NCT00954733 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00954733 about?

NCT00954733 is a clinical study titled "A Comparison of the Detection of Hypoventilation During Deep Sedation Utilizing Nasal End Title CO@ Versus Transcutaneous CO2 Measurement Techniques". The estimation of the partial pressure of carbon dioxide (PCO2) in the arterial blood is used to judge the adequacy of ventilation during spontaneous and controlled ventilation. Although the gold standard for monitoring PCO2 remains arterial blood gas sampling, this requires an invasive procedure an...

What is the current status of trial NCT00954733?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2009-06. Estimated completion is 2009-08.

What interventions are being tested in trial NCT00954733?

The interventions under investigation include: Arterial blood draw (OTHER).

Who is sponsoring clinical trial NCT00954733?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00954733's enrollment target sits among peer trials

40 1447th of 2000 higher than 465 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00954733, the US trial registry maintained by the National Library of Medicine. NCT00954733 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.