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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01565226
Other study ID # D007171
Secondary ID
Status Completed
Phase N/A
First received March 25, 2012
Last updated November 1, 2016
Start date August 2012
Est. completion date February 2015

Study information

Verified date November 2016
Source Medtronic - MITG
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

- This will be an observational study. Respiratory data will be recorded using Capnostream20p. There will be no use in the recorded data for the medical care of the patients. Other clinical data will be captured in the CRF. Similar study is currently conducted in Bnai Zion MC since 2008. Thirty four (34) patients have been recruited without any adverse events.

- During the study the medical team will capture in the CRF the following: Blood gas and distal capnography values at time of sampling, ventilator settings at time of sampling.

- Changes made in the ventilation parameters, blood gas time and results, concomitant treatment (e.g. suction) and concomitant medication (respiratory related e.g. surfactant), vital signs all these will be retrieved from the patient's medical charts.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Intubated neonates with double-lumen ETT (Uncuffed Tracheal Tube, Mallinckrodt Inc., Chih, Mexico)

- Neonates that their respiratory condition requires HFV

- Neonates expected to have at least 3 pairs of distal capnography measurements and blood gas samplings.

Exclusion Criteria:

- Intubated neonates with single-lumen ETTs

- Neonates who are ventilated with conventional ventilation

- Any significant medical condition which, at the investigator's discretion, may interfere with the study.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Intubated Neonates That Require High Frequency Ventilation

Locations

Country Name City State
Israel Soroka MC Beer Sheva
Israel Bnai Zion MC Haifa
Israel Shaare Zedek MC Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Oridion

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate the feasibility of measuring distal capnography on HFV and to assess its correlation and agreement with PaCO2 in infants ventilated with HFV in a prospective study. August 2012 - February 2015 No