Actively Recruiting
Proof of Principle Study for an Efficacy Trial of Linaclotide for Cystic Fibrosis
Led by University of Nottingham · Updated on 2026-05-06
26
Participants Needed
1
Research Sites
29 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Linaclotide is a medicine used to treat constipation and irritable bowel syndrome with constipation (IBS-C). It works by acting on the surface of the gut lining, where it increases the movement of salt and water into the bowel. This softens stools, makes them easier to pass, and can also reduce gut pain One advantage of linaclotide is that, unlike some natural substances in the gut, it is stable and can act throughout the intestine. Studies in animals show that it has the strongest effect in the upper small intestine, but it may act in other parts of the bowel as well. In people, however, it is not yet clear whether linaclotide mainly works in the small intestine or in the large intestine (colon). Knowing this is important, because it could help the investigators understand whether linaclotide might also be useful in other conditions, such as cystic fibrosis, where the gut does not handle fluid properly. Linaclotide is taken as a capsule, but less than 1% is absorbed into the bloodstream. Instead, it stays in the gut, where it is broken down into smaller active parts. This means both the small intestine and colon may be exposed to its effects. Until now, it has been hard to study this because traditional methods only measure one part of the gut at a time. A team at the University of Nottingham has developed MRI scanning methods that can safely and non-invasively measure water content in the small intestine and colon. The aim of this pilot study is to use MRI in healthy volunteers to see exactly where linaclotide acts. This knowledge will help optimise future studies in conditions such as cystic fibrosis.
CONDITIONS
Official Title
Proof of Principle Study for an Efficacy Trial of Linaclotide for Cystic Fibrosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Willing and able to give informed consent for participation
- Not currently taking any medications except SSRIs, low dose tricyclic antidepressants, antihistamines, or oral contraceptive pill
- Aged between 18 and 60 years
- Able to follow the study protocol including fasting, lifestyle restrictions, taking linaclotide or placebo, MRI scanning, consuming test meal, and recording stool frequency and appearance
You will not qualify if you...
- Contraindications to MRI scanning such as metallic implants, pacemakers, metal in eyes, or inability to lie still for 5 minutes
- Pregnant, breastfeeding, or planning pregnancy during the study
- History of gastrointestinal disorders affecting bowel function
- Previous resection of esophagus, stomach, or intestine (except appendix)
- Having an intestinal stoma
- Medical conditions that compromise study participation including food intolerance or contraindications to linaclotide or placebo
- Body mass index less than 18.5 or greater than 35
- Unwillingness to follow dietary and lifestyle restrictions
- Unable to stop drugs that alter GI motility during the study
- Current or recent (past 3 months) use of antibiotics or probiotics
- Night shift work during the week before study day
- Cognitive dysfunction, chaotic lifestyle related to substance abuse, or inability to comply with protocol
- Participation in another research study in last 3 months involving invasive procedures or inconvenience allowance
AI-Screening
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Trial Site Locations
Total: 1 location
1
Sir Peter Mansfield Imaging Centre
Nottingham, United Kingdom, NG7 2QX
Actively Recruiting
Research Team
J
Josh Thorley, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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