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)

Cedar Valley Digestive Health Center

Waterloo, Iowa, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06460038


Related Trials