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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02673307
Other study ID # 2016-A00009-42
Secondary ID L15-206
Status Completed
Phase N/A
First received February 1, 2016
Last updated October 13, 2016
Start date March 2016
Est. completion date October 2016

Study information

Verified date October 2016
Source Hôpital Edouard Herriot
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

The aims of this prospective cross over study was to compare the gastric emptying of 250 ml water in fasting volunteers, in two situations : without chewing gum or while chewing gum during 45 min


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date October 2016
Est. primary completion date October 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ASA 1 or 2 volunteers

Exclusion Criteria:

- digestive diseases, gastroparesis

- Smokers

- Pregnancy

- Diabetes Mellitus

- Medication affecting gastric motility

- Previous gastrointestinal surgery

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Basic Science


Related Conditions & MeSH terms

  • Comparison of Gastric Emptying Rate of Water When Chewing Gum or Not

Intervention

Behavioral:
1 chewing gum over 45 minutes


Locations

Country Name City State
France Hopital Femme Mère Enfant - Hospices Civils de Lyon Bron

Sponsors (1)

Lead Sponsor Collaborator
Lionel Bouvet

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of the rate of gastric emptying of 250 ml water when chewing or not chewing gum, as assessed by the ultrasound measurement of antral area performed each 20 min every 20 minutes during 120 min No