palatability
Conditions
Interventions
The test sample (MOVICOL Combination Powder LD + organoleptic masking agents) is dissolved in 10 mL of water. The solution is held in the mouth for 10 seconds and then spit out. After spitting out, vo
Sponsors
Tatsuguchi Mariko
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy volunteers, 18 years of age or older (both male and female)
Exclusion criteria
Exclusion criteria: 1. Volunteers with obvious taste disorders 2. Volunteers with self-reported oral abnormalities such as stomatitis 3. Volunteers with a history of allergy to the ingredients of Movicol oral powder 4. Volunteers with confirmed or suspected diseases for which Movicol oral powder is contraindicated (intestinal obstruction, intestinal perforation, severe inflammatory bowel disease such as ulcerative colitis, Crohn's disease, or toxic megacolon) 5. Volunteers who are pregnant, possibly pregnant, or breastfeeding 6. Any other volunteers deemed inappropriate by the principal investigator or co-investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS score of overall palatability | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS score of bitterness, VAS score of sweetness, VAS score of sourness, VAS score of saltiness, VAS score of smell and recommendation for children to take | — |
Contacts
Public ContactMariko Tatsuguchi
Hamamatsu University School of Medicine
Outcome results
None listed