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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02938065
Other study ID # 2016-0566
Secondary ID
Status Completed
Phase N/A
First received July 25, 2016
Last updated August 21, 2017
Start date June 2016
Est. completion date June 2017

Study information

Verified date August 2017
Source Children's Hospital Medical Center, Cincinnati
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The proposed study will use this technology to observe emptying of the stomach of a protein and carbohydrate rich clear liquid sports/nutrition drink.


Description:

In order to ensure safety for elective anesthesia, standard practice requires pre-operative fasting to ensure that the stomach is empty prior to induction. The question of timing of pre-operative consumption of oral fluids remains vexed, and challenges anesthesiologists on a frequent basis. In the past few years, a new controversy in pre-operative fasting has arisen: clear drinks with increased content of protein and carbohydrate have been introduced to the market. Families and professionals alike are confused whether to regard these products as clear liquids (2 hours fasting) or as solids (at least 6 hours).

Ultrasound is now considered an accepted tool in the anesthesia literature as a surrogate for aspiration risk with different materials and in different disease states.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date June 2017
Est. primary completion date June 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years to 14 Years
Eligibility Inclusion Criteria:

- 8-14 years old

- Willing to not eat or drink for at least 8 hours overnight beforehand

- Have a BMI < 35

Exclusion Criteria:

- Use tobacco of any kind

- Taking any medications (Females: oral contraceptives okay)

- Suffers from diabetes, Crohn's Disease, Celiac Disease, Malabsorption, Galactosemia

- Has ever has surgery on esophagus, stomach, or small bowel

- Has allergies or intolerances to milk, apple juice, or ensure clear

- Has any surgical condition, disease, or on any medication that could alter stomach emptying rate

- Has any disease that limits day-to-day activities

- Is pregnant or possibly could be pregnant

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Ultrasound
Baseline ultrasound is performed upon arrival. Ultrasound is performed when beverage is consumed and then every 30 minutes thereafter until stomach is empty.
Other:
2% milk
16 participants will drink 10 ounces of 2% milk
apple juice
16 participants will drink 10 ounces of apple juice
ensure clear
16 participants will drink 10 ounces of ensure clear

Locations

Country Name City State
United States Cincinnati Children's Medical Center Cincinnati Ohio

Sponsors (1)

Lead Sponsor Collaborator
Children's Hospital Medical Center, Cincinnati

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measurement of rate of gastric emptying through measure of the gastric antral cross-sectional area (CSA) Participants will be followed up to 6 hours after drinking 10 ounces of beverage
Primary Subjective evolution of hunger after ingestion of clear fluids using a validated visual analog scale called the Hunger Satiety Score Participants will be followed up to 6 hours after drinking 10 ounces of beverage
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