Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02866123
Other study ID # Couteau-Girard 2014
Secondary ID
Status Terminated
Phase N/A
First received August 4, 2016
Last updated August 12, 2016
Start date January 2015

Study information

Verified date July 2016
Source Centre Hospitalier Universitaire Dijon
Contact n/a
Is FDA regulated No
Health authority France: Agence Nationale de Sécurité du Médicament et des produits de santé
Study type Interventional

Clinical Trial Summary

There are several ways to verify the correct positioning of a gastric tube. Radiography is considered the reference method. The use of ultrasonography could diminish the number of radiographies necessary. The hypothesis of this research is that gastric ultrasonography performed during insertion of the tube is a reliable examination to check the correct positioning of gastric tubes in intensive care.


Recruitment information / eligibility

Status Terminated
Enrollment 19
Est. completion date
Est. primary completion date May 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients, or their persons of trust, in cases of coma or sedated patients) who have given informed oral consent

- All patients hospitalized in the surgery intensive care unit of Dijon CHU, who are intubated and require a gastric tube

Exclusion Criteria:

- Adults under guardianship, patients under 18 years of age

- Patients without national health insurance cover

- Pregnant women

- Wound or dressing preventing gastric ultrasonography (laparotomy is not an exclusion criterion if the dressing does not prevent ultrasonography being performed)

- result of the radiographic verification seen before the gastric ultrasonography is done

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
ultrasonography

Radiation:
pulmonary radiography


Locations

Country Name City State
France CHU Dijon Bourgogne Dijon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of ultrasonography examinations validating the correct insertion of a nasogastric tube (NGT) Day 1 No