CClinicalTrials.gg
Status unknownNCT00208000Updated Nov 29, 2010

A Clinical Double Blind, Randomized Study of the Efficacy of Hyperuricemia Treatment With Anserine Product.

A Phase 2 interventional study of Marine active in "Hyperuricemia,Anserine", sponsored by China Medical University Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2010-11-29.

Sponsored by China Medical University Hospital · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2005), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

Hyperuricemia is a common metabolic disorder.The Yaizu Suisankagaku Industry Company have developed industrial production named Marine Active, was able to offer anti-fatigue activity by animal trial data. Human clinical trials showed reduced creatine phosphokinase activity and a sero-uric acid reduction activity was also observed. So we are committed to design the clinical randomized, double blind study about hyperuricemia management with Marine Active. All these efforts are hoped to find a novel method to manage hyperuricemia.

Read the detailed description

Hyperuricemia is a common metabolic disorder. It can result from a decreased renal uric acid excretion, increased urate production, or both. The classical association with clinical gout is well-known. The principal indications for uric acid-lowering therapy, including allopurinol, probenecid and sulfinpyrazone, are the patients with gout history, macroscopic subcutaneous tophi, frequent attacks of gouty arthritis, or a documented state of uric acid overproduction. Hyperuricemia without gout attack is not an indication for treatment.However, hyperuricemia is often associated with other cardiovascular disease risk factors such as obese, hyperlipidemia, glucose intolerance and hypertension. It is known a symptom of syndrome X (also known as multiple risk factor clustering syndrome). Diet control is the only way to control serum uric acid level, but always it is not enough. So how to management hyperuricemia is important and is a potential management.Histidine-containing dipeptides such as Anserine and Carnosine have been studied extensively in recent years. These dipeptides were shown to be effective in acting as buffering agents against protons developed during anaerobic exercise. Anserine and Carnosine also have strong anti-oxidant activity, anti-cancer activity, immuno-response modulation, fat reduction and enhanced wound healing functions. The Yaizu Suisankagaku Industry Company have developed industrial production process to extract and purify the dipeptides from Bonito and Tuna. The extract, named Marine Active, was able to offer anti-fatigue activity by animal trial data. Human clinical trials showed reduced creatine phosphokinase activity and a sero-uric acid reduction activity was also observed. So we are committed to design the clinical randomized, double blind study about hyperuricemia management with Marine Active. All these efforts are hoped to find a novel method to manage hyperuricemia.

02

Conditions studied

  • "Hyperuricemia,Anserine"

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03

In context

Hyperuricemia

215 studies on the registry are indexed under Hyperuricemia; 40 are open to participants now.

Browse Hyperuricemia studies →

Lead sponsor

China Medical University Hospital is the lead sponsor of 464 studies on the registry; 116 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Male or female patients, age between 18 to 60 years
  • With the data of serum uric acid level more than 8.0 mg/dl within 2 weeks before the initiation of study
  • Signed informed consent obtained prior to inclusion into the study

Exclusion criteria

Exclusion Criteria:

  • Pregnant women.
  • Acute onset of gouty arthritis or renal stone
  • Significant liver or renal dysfunction, hematological disease, oncological disease, or other life threatens disorders.
  • Condition that need the management of diuretics or analgesics agent
  • Have been administrated by anti-hyperuricemia agent or healthy food with in 4 weeks before the initiation of study.
  • The serum uric acid level could be decrease to lower than 8 mg/dl by diet control.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double

Interventions

  • DrugMarine active
06

Study locations

1 of 1 sites recruiting
  • China Medical University Hospita
    Taichung, 404, Taiwan
    Recruiting
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 29, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00208000
Lead sponsor
China Medical University Hospital
First posted
Sep 21, 2005
Start date
Jul 2004
Completion
Apr 2006 (estimated)
Last update
Nov 29, 2010

Study contacts

Chiu-Shong Liu, Director
Contact
huangimd@lsc.net.tw
886-4-22052121 ext. 5068
Kuo-Chin Huang
Contact
huangimd@lsc.net.tw
886-4-22052121 ext. 5068
Chiu-Shong Liu, Director
principal investigator · Family Medicine, China Medical University Hospital
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2005. You cannot join it, but the record below documents what was studied.

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