The purpose of this study is to evaluate the effect of varenicline on rectal sensation, based on ascending method of limits and on graded rapid phasic distensions in participants with non-constipation IBS and chronic abdominal pain.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
8
Initial, 0.5 mg orally once daily for 3 days, then 0.5 mg every 12 hours on days 4 through 7, and then 1 mg in morning of day 8. Medication is taken after eating and with a full glass of water.
Mayo Clinic in Rochester
Rochester, Minnesota, United States
Rectal compliance
Pressure-volume relationship of rectum during balloon distension
Time frame: Comparison on day 8 of vareniciline treatment compared to baseline
Rectal sensation thresholds during ascending method of limits
Report of rectal sensation during balloon distension 0-44mmHg
Time frame: Comparison on day 8 of vareniciline treatment compared to baseline
Rectal sensation ratings during random order, graded phasic distensions
Report of rectal sensation during balloon distensions
Time frame: Comparison on day 8 of vareniciline treatment compared to baseline
Safety/adverse effects
Safety/adverse effects during administration of varenicicline
Time frame: 8 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.