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CompletedNCT01359176Updated Apr 26, 2016

Capnography Data Collection From Healthy Participants

An observational study in Healthy Volunteers, sponsored by Shaare Zedek Medical Center. Completed at 1 site in Israel. Open to participants aged 1 Year and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-04-26.

Sponsored by Shaare Zedek Medical Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
160
Ages
1 Year and older
Sex
All
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Study summary

Capnography is the non-invasive monitoring of the concentration or partial pressure of carbon dioxide (CO2) in the expired respiratory gases; it is thus a non-invasive monitoring technique which allows fast and reliable insight into ventilation, circulation and metabolism. The capnogram is a direct monitor of the inhaled and exhaled concentration or partial pressure of CO2, and an indirect monitor of the CO2 partial pressure in the arterial blood. The purpose of this study is to create a waveform library by collecting CO2 waveform data from healthy volunteers.

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Conditions studied

  • Healthy Volunteers
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In context

Lead sponsor

Shaare Zedek Medical Center is the lead sponsor of 191 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
1 Year and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Adult and pediatric healthy volunteers

Inclusion criteria

  • Consent to participate in the trial by volunteer themself or by their legal guardian

Exclusion criteria

Exclusion Criteria:

  • Any individual who does not consent themselves or their legal guardian does not grant consent to participate in the trial
  • A medical history of heart disease, lung disease, smoking, hypertension, pregnancy, diabetes or any other illness that excludes the participant from enrolling in the trial in the opinion of the PI
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
160 participants (actual)

Groups and cohorts

  • Healthy volunteers
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What researchers measure

Primary outcomes

  1. To gather data received from monitoring healthy participants as reference for the creation of a capnography waveform library.

    Participants will put on the capnography monitoring device (a simple tube with prongs that fit in the nostrils, similar in design to the oxygen delivering device "nasal cannula") and this device will be hooked up to a computer. The participants will be asked to do very simple activities, such as sit, stand, eat and drink. The changes in their CO2 waveforms during these activities will be recorded in order to build a library of reference waveforms.

    Time frame: One hour

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Study locations

1 site
  • Shaare Zedek Medical Center
    Jerusalem, 91031, Israel
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 26, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01359176
Lead sponsor
Shaare Zedek Medical Center
Responsible party
Sponsor
First posted
May 24, 2011
Start date
May 2010
Primary completion
Aug 2014
Completion
Jan 2015
Last update
Apr 26, 2016

Study contacts

Sharon Einav, MD
principal investigator · Shaare Zedek Medical Centre

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2010. You cannot join it, but the record below documents what was studied.

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