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OpenTrials
Completed

NCT Number: NCT04092049

Lollipop on Gastric Emptying

To investigate the effect of chewing lollipop on gastric volume and gastric emptying in healthy volunteers drinking water.

Completed

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Key information

Conditions

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Xijing Hospital

Xi'an, Shaanxi, 710032, China

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • volunteer aged 18 years-45 years old
  • volunteer with a body mass index between 18 and 28 kg/m2

Exclusion criteria

  • those with history of diabetes mellitus
  • those with gastric diseases
  • those with history of gastro-intestinal surgery
  • those with history of smoking
  • those with use of gastric mobility medicines
  • those with pregnancy or breeding

Treatment and study plan

Lollipop

Other

chewing lollipop for 10 minutes

Primary outcomes

  1. half time of gastric emptying

    Time frame: from drinking water to gastric volume return to half of top volume before drinking water,on an average of 2 hours

Secondary outcomes

  1. time of gastric emptying

    Time frame: from drinking water to gastric volume return to baseline before drinking water,on an average of 2 hours

Sponsors and collaborators

Lead sponsor

Air Force Military Medical University, China

Other

Registry information

Official study title

Effect of Chewing Lollipop on Gastric Emptying

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Sep 17, 2019
Registry last updated
Apr 17, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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