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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01087047
Other study ID # MAVAG
Secondary ID
Status Completed
Phase N/A
First received March 10, 2010
Last updated June 11, 2012
Start date March 2010
Est. completion date March 2012

Study information

Verified date June 2012
Source Club d'Anesthésie-Réanimation Pédiatrique Armand Trousseau
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Observational

Clinical Trial Summary

It is well known that airway management can be difficult during pregnancy. Increased risks for difficult intubation in pregnant women have been often reported. Thus, pregnancy is regarded as a period of high anesthesiologic risk.

Generalized weight gain is a well known factor influencing the upper airway in pregnant women. However, the modifications of the airway itself are less well documented.

The acoustic reflection method is based on the analysis of the reflection of a single transient planar wave allowing the analysis of the longitudinal cross-sectional area profile of the examined cavity. It is a noninvasive and harmless method.

The aim of the study is to evaluate by acoustic reflection method the physiological modifications of the upper airways during pregnancy.

Women enrolled in the study will undergo an acoustic recording during the first, second, and third trimester of pregnancy, as well as two days and one month after delivery. Forty pregnant women will be included in this monocentric, prospective, open labelled study.

Moreover, a single acoustic recording will be performed in 10 other pregnant women undergoing an MRI for obstetrical purpose. The estimated caliber of the upper airways by MRI and acoustic method will be compared.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 2012
Est. primary completion date March 2012
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Pregnant women who attend the routine ultrasound control in our institution before 14 weeks of pregnancy will be invited to participate in the study.

- Women are eligible for the study if they are:

- healthy (no previous disease, hypertension, nor obesity),

- 18 years or more

- with a singleton live fetus at the routine ultrasound scan

- with a normal pregnancy.

Exclusion Criteria:

- Pregnancy complications

- Multiple pregnancy

- High risk for preterm labor

- Underlying diseases that could interfere with the results (such as pre-existing upper airway problems) and participation.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Acoustic reflection method
An acoustic reflection device gives the longitudinal cross-sectional area profile along airways. It is based on the analysis of a planar acoustic wave propagating in a rigid duct connected to airway.

Locations

Country Name City State
France Armand Trousseau University Hospital Paris
France Hôpital d'Enfants Armand Trousseau Paris

Sponsors (2)

Lead Sponsor Collaborator
Club d'Anesthésie-Réanimation Pédiatrique Armand Trousseau Institut National de la Santé Et de la Recherche Médicale, France

Country where clinical trial is conducted

France, 

References & Publications (2)

Kodali BS, Chandrasekhar S, Bulich LN, Topulos GP, Datta S. Airway changes during labor and delivery. Anesthesiology. 2008 Mar;108(3):357-62. doi: 10.1097/ALN.0b013e31816452d3. — View Citation

Louis B, Fodil R, Jaber S, Pigeot J, Jarreau PH, Lofaso F, Isabey D. Dual assessment of airway area profile and respiratory input impedance from a single transient wave. J Appl Physiol (1985). 2001 Feb;90(2):630-7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Physiological modifications during pregnancy and acoustic reflection method Main aim: to evaluate by acoustic reflection method the physiological modifications of the upper airways during pregnancy. Women enrolled in the study will undergo an acoustic recording during:
the 1st, 2d, and 3d trimester of pregnancy
two days after delivery
one month after delivery
6 months No
Secondary MRI and acoustic reflection method Secondary aim: a single acoustic recording will be proposed to 10 pregnant women undergoing an MRI for obstetrical purpose.
The estimated caliber of the upper airways by MRI and acoustic method will be compared.
6 months No
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