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UnknownNCT06084585

The Efficacy of Amway Uric Acid Lowering Product on Hyperuricemia

A Three Arms, Randomized, Double-blind Controlled Trial of the Efficacy of Amway Uric Acid Lowering Product on Hyperuricemia

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
180 (estimated)
Sponsor
Amway (China) R&D Center · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The goal of this three arms, randomized, double-blind controlled interventional study is to evaluate the efficacy of Amway uric acid lowering product improving hyperuricemia in patients aged 18 and 65 years old. The main question it aims to answer is: \- whether the serum uric acid level of patients with hyperuricemia could be significantly lowered after 3 months intervention with Amway uric acid lowering product 180 eligible participants will be enrolled in one study site and randomized to three study groups (two product group and one placebo group), who will consume the assigned products for 3 months and be arranged to 3 site visits. All relevant clinical data will be captured and recorded into CTMS (Clinical Trial Management System) for statistical analysis and reporting. Researchers will compare the three study groups to conclude how Amway uric acid lowering product will improve hyperuricemia.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTStudy Product A (High-dose 2X)participants in this arm will consume 1 sachet of this product with 200ml water per time, once a day after meal, for 3 months
DIETARY_SUPPLEMENTStudy Product B (Low-dose X)participants in this arm will consume 1 sachet of this product with 200ml water per time, once a day after meal, for 3 months
DIETARY_SUPPLEMENTPlaceboparticipants in this arm will consume 1 sachet of this product with 200ml water per time, once a day after meal, for 3 months

Timeline

Start date
2023-10-23
Primary completion
2024-02-28
Completion
2024-03-15
First posted
2023-10-16
Last updated
2023-10-16

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06084585. Inclusion in this directory is not an endorsement.