Clinical Trials Directory

Trials / Unknown

UnknownNCT06320379

Zypan Functional Dyspepsia

Evaluating Changes in Quality of Life and Digestion in Functional Dyspepsia in Adults

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
64 (estimated)
Sponsor
National University of Natural Medicine · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the effects of a readily available dietary supplement on quality of life and digestion in adults with functional dyspepsia.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTZypanThe study product is a dietary supplement manufactured by Standard Process Inc (i.e., Zypan®). One serving (i.e., two tablets) contains a proprietary blend (595 mg) of the following: Betaine hydrochloride, bovine pancreas Cytosol™ extract, pepsin (1:10,000), pancreatin (3x), stearic acid (vegetable source), ammonium chloride, bovine spleen, and ovine spleen. Non active ingredients will include cellulose and calcium stearate. Participants will be instructed to take two tablets three times daily with meals
DIETARY_SUPPLEMENTPlacebo ComparatorThe control supplement will not contain any of the active ingredients in Zypan® and will also be manufactured by Standard Process Inc. Two tablets will contain 435 mg of cellulose (42%), 288 mg rice bran powder (28%), 201 mg of calcium lactate powder (19.5%\*), 103 mg citric acid (10%), and 2.6 mg calcium stearate (0.25%)

Timeline

Start date
2023-03-15
Primary completion
2024-12-31
Completion
2024-12-31
First posted
2024-03-20
Last updated
2024-08-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06320379. Inclusion in this directory is not an endorsement.