An interventional study of Linaclotide and Placebo in Irritable Bowel Syndrome With Constipation (IBS-C), sponsored by Augusta University. Completed at 1 site in United States. Open to participants aged 18 Years to 64 Years. Per ClinicalTrials.gov, last updated 2018-07-23.
Sponsored by Augusta University · Not applicable, Interventional, and Other
The purpose of this study is to understand how a drug called Linaclotide improves bowel function and abdominal pain in patients with Irritable Bowel Syndrome with Constipation (IBS-C) as well as to examine whether Linaclotide alters communication between the brain and pelvic-floor region.
Linaclotide has been shown to improve abdominal pain and bowel symptoms in IBS-C, and is approved by the FDA for the treatment of this condition. However, how exactly this drug works to relieve abdominal pain and discomfort in humans is not clearly known. Studies in animal models suggest that patients with IBS-C have hypersensitivity in the gut.
Consequently, in IBS-C patients, there is rapid and excessive conduction of signals both from the brain and central nervous system region towards the pelvic-floor (anorectal axis) and the reverse direction. The investigators hypothesize that treatment with Linaclotide may improve/normalize these signals and thereby improve bowel symptoms.
Investigators will test this theory using a new, noninvasive (and established) method of studying this communication pathway between the brain and gut.
modulate these mechanisms and thereby improve visceral pain.
Investigators propose three specific aims:
1,062 studies on the registry are indexed under Irritable Bowel Syndrome; 190 are open to participants now.
This study's enrollment of 39 is below the median of 71 across 853 interventional studies indexed under Irritable Bowel Syndrome.
Browse Irritable Bowel Syndrome studies →Augusta University is the lead sponsor of 177 studies on the registry; 24 are open to participants now.
Of its 10 completed or terminated interventional studies of FDA-regulated products, 3 (30%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Linaclotide 290micrograms q day 30 min before meal for a 10 week period
Drug: Linaclotide
Placebo q day 30 min before meal for a 10 week period
Drug: Placebo
1: Change from baseline in Prolongation and normalization of anal CEP and rectal CEP responses at 10 weeks.
A rectal catheter will be inserted into the rectum, up to 10 cm from the anal verge. The threshold for first sensation and pain will be determined by increasing the electrical stimulation in steps of 1 mA. subsequent stimuli will be applied at an intensity of 75% of the difference between the first sensation and pain thresholds. The CEPs will be recorded in a quiet room in a semi-recumbent position. Four runs of 50 stimuli will be averaged for both the rectal and anal stimulation studies, with a 5-min rest period between each run and a 30 minute rest period between rectal and anal studies.
Time frame: at baseline assessment and at 10 weeks following baseline
Change from Baseline in Prolongation and normalization of rectal MEP and anal MEP at 10 weeks.
A 70 mm figure of eight coil, positioned over the cranium's vertex. TThe coil will be placed with the anterior edge of the cross point over the region of interest, with the handle pointing backward (for midline grid points) or at an angle of 45º tangential to the scalp surface (for lateral grid points). We will perform TMS of the anorectal motor cortex and assess the anal and rectal MEPs (EMG), by using the anorectal probe.
Time frame: at baseline assessment at at 10 weeks following this baseline assessment
This study is completed, as verified in Jul 2018. You cannot join it, but the record below documents what was studied.
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