RecruitingPhase 2NCT06460038
Tenapanor in Synucleinopathy-Related Constipation
Efficacy and Safety of Tenapanor in Synucleinopathy-Related Constipation
Sponsor
Cedar Valley Digestive Health Center
Enrollment
30 participants
Start Date
Jan 1, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
Investigation of tenapanor as a potential treatment for synucleinopathy-associated constipation
Eligibility
Min Age: 50 YearsMax Age: 89 Years
Inclusion Criteria5
- Age 50-89 years.
- Diagnosis of PD within Hoehn and Yahr stages 1-3, confirmed by a neurologist per International Parkinson and Movement Disorder Society criteria.
- Average weekly stool frequency of ≤5 spontaneous bowel movements (SBMs) and ≤2 complete spontaneous bowel movements (CSBMs) over the past 6 months. These criteria will be verified during a 2-week screening period.
- Stool consistency ≤3 on the Bristol Stool Form Scale (BSFS). This criterion will be verified during a 2-week screening period.
- Agreement to use contraception, if applicable.
Exclusion Criteria5
- Functional diarrhea or IBS-D/M based on Rome IV Criteria.
- Symptomatic structural GI abnormalities or inflammatory bowel disease.
- Significant hepatic (ALT or AST ≥ 2.5x the upper limit of normal) or renal (serum creatinine \>2mg/dl) dysfunction.
- Pregnancy or lactation.
- Diagnosis of primary dyssynergic defecation by anorectal manometry.
Interventions
DRUGTenapanor
Inhibitor of NHE3
DRUGPlacebo
Placebo drug
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06460038
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