Constipation Clinical Trial
— KIWIOfficial title:
Effect of Kiwifruit on Gastrointestinal Fluid Distribution and Transit in Healthy Volunteers
NCT number | NCT03303417 |
Other study ID # | A200317 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 27, 2017 |
Est. completion date | June 1, 2018 |
Verified date | March 2019 |
Source | University of Nottingham |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Constipation is a widespread and common problem in which a person finds it difficult and/or
painful to open their bowels. The current treatment is the use of medications called
laxatives. Kiwifruit is a widely available food that has been shown to possess some laxative
properties. The cause of this is unknown. Non-invasive medical imaging techniques such as
Magnetic Resonance Imaging now allow taking pictures of the gut and its contents. The
Nottingham GI MRI research group specialises in these techniques and in this study use such
images to assess the changes induced in the gut contents by kiwifruit to improve
understanding of how it helps patients with constipation.
The volunteers will be asked to undergo 2 studies in which they take either kiwifruit or
placebo (sugary drink) two times a day for 2 days and then spend a study day where will they
will be fed some more kiwifruit/placebo and some normal food and image their gut at
intervals. Participants will be asked to complete a stool diary to determine if they
experience a laxative effect.
Status | Completed |
Enrollment | 16 |
Est. completion date | June 1, 2018 |
Est. primary completion date | November 1, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Healthy volunteers scoring within the normal range for bowel symptoms as assessed using the GSRS, aged 18-65 years. Exclusion Criteria: 1. Inability to discontinue medication likely to alter GI transit. 2. Previous gastrointestinal surgery (excluding cholecystectomy and appendectomy). 3. Known inflammatory bowel disease, coeliac disease. 4. Known intolerance of kiwifruit. 5. Inability to discontinue drugs likely to alter gut transit. 6. Subjects considered by the investigator unlikely to comply with study protocol. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | University of Nottingham | Nottingham | Nottinghamshire |
Lead Sponsor | Collaborator |
---|---|
University of Nottingham | Zespri International Limited |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Relaxation Time in Ascending Colon | Area under curve of Ascending colon T1 measured on MRI , in milliseconds. Measurements at 0, 1, 2, 3, 4, 5, 6, 7, and 8 hours post-intervention | 0 - 8 hours | |
Secondary | Small Bowel Water Content Measured by MRI, in mL | Area under the curve of change of small bowel water, 0-8 hours, measured by MRI, in mL Measurements at 0, 1, 2, 3, 4, 5, 6, 7, and 8 hours post-intervention | 0 - 8 hours | |
Secondary | Colonic Volume | Ascending (AC), transverse (TC) and descending (DC) colonic volumes, measured by MRI, in mL Data given: AUC for total colon Measurements at 0, 1, 2, 3, 4, 5, 6, 7, and 8 hours post-intervention | 0 - 8 hours | |
Secondary | Colonic Transit Time | Transit of markers through gut as assessed by the weighted average position score (total score 0-7, calculated from a score of 0-7 of each of the 5 marker pills) at 24 h on MRI A lower score indicates faster transit. | 24hr | |
Secondary | Bowel Habit | Assessment, via Diary, of bowel frequency Data given: stool frequency | 7 days |
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