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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04288466
Other study ID # tccandre2020
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 1, 2020
Est. completion date July 1, 2020

Study information

Verified date February 2020
Source Brasilia University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Gastric volume will be measured before, 5, 30, 60, 90 and 120 min after drinking 450ml of maltodextrin in young adults and elderly.


Description:

Gastric volume will be estimated before, 5, 30, 60, 90 and 120 min after drinking 450ml of maltodextrin in young adults and elderly using antral ultrasound.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date July 1, 2020
Est. primary completion date April 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ASA physical status I or II;

- No known risk factor for slow or fast gastric emptying.

Exclusion Criteria:

- Vomiting the study solution before completion.

- Wrong timing of assessment.

- Protocol violation.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
maltodextrin
maltodextrin solution 450ml

Locations

Country Name City State
Brazil Hospital das Forças armadas Brasilia Distrito Federal

Sponsors (1)

Lead Sponsor Collaborator
Brasilia University Hospital

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Antral Volume change Antral volume in cm² assessed by ultrasound in semirecumbent position. Just before and 5, 30, 60, 90 and 120 minutes after drinking the study solution (repeated measures)
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