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Status unknownNCT03473951Updated Jun 9, 2020

The Relationship Among, Serum Uric Acid, Left Ventricular Hypertrophy and Metabolic Syndrome

An observational study in Hyperuricemia and Healthy, sponsored by National Defense Medical Center, Taiwan. Status unknown at 1 site in Taiwan. Open to participants aged 20 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-06-09.

Sponsored by National Defense Medical Center, Taiwan · Observational

The sponsor has not verified this record recently (last verified Jun 2020), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
18,000
Ages
20 Years to 65 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 14 studies in Hyperuricemia with a site in Taiwan — 1 open to participants now, 1 under way, none of them phase 3. Hyperuricemia · Taiwan.

Started
2018
the only one that year
Observational
3 of 14
none open now
Registered
5th of 14
by date
Lead sponsor
3 of 14
National Defense Medical Center, Taiwan

Among the 14 studies in Hyperuricemia with a site in Taiwan, this one is the only one that started in 2018, is one of 3 observational ones, and was the 5th registered.

Hyperuricemia

240 studies on the registry are indexed under Hyperuricemia; 44 are open to participants now.

This study's planned enrollment of 18,000 is above the median of 183 across 40 observational studies indexed under Hyperuricemia.

Browse Hyperuricemia studies →

Open to participants now

1 of the 14 studies in Hyperuricemia with a site in Taiwan is open now, in 2 countries. Each count lists the studies.

Who these studies take

Of the 29 Hyperuricemia studies recruiting now, 8 (28%) set no upper age limit and 13 (45%) stop at 75 or younger; 1 take children under 18; 6 take healthy volunteers.

This study: 20 Years to 65 Years · all sexes · healthy volunteers too.

The full table on the hub →
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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 14 studies in Hyperuricemia with a site in Taiwan, or all of them as a file.
02

Study summary

Hyperuricemia is associated with the prevalence of metabolic syndrome and cardiovascular risks in diverse of the population. Whether the dose-response effects on the prevalence of metabolic syndrome and cardiometabolic risks is unclear. The present study is conducted to investigate the relationship between serum uric acid and the prevalence metabolic syndrome and left ventricular hypertrophy.

Read the detailed description

Apparently healthy individuals with an estimated screening number of approximately twenty-thousand individuals undergo an annual health exam in the investigators' hospital. The routine exam includes measurements of body height, body weight, blood pressure, visual and acoustic acuity, physical examinations, basic blood tests, urine analyses, chest radiography, and electrocardiography. The blood tests were performed after individuals fasted for at least eight hours. Individuals with any abnormal results underwent a clinical examination at an outpatient department for safety issues, ensuring the accuracy of the data. All data were registered prospectively. The investigators retrospectively collected data from the annual exam.

03

Conditions studied

  • Hyperuricemia
  • Healthy

Keywords

  • Hyperuricemia
  • Metabolic syndrome
  • Left ventricular hypertrophy
04

Who can participate

Ages eligible
20 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Apparently healthy individuals routinely underwent the annual health exam.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Individuals with ages of 20-65 years underwent the annual health exam at the investigators' hospital.

Exclusion criteria

Exclusion Criteria:

  • The individual had no data to define metabolic syndrome, including waist circumference, office blood pressure, serum uric acid, triglyceride, high-density lipoprotein cholesterol, fasting glucose.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
18,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Hyperuricemia

    Hyperuricemia is defined as a serum uric acid level of 7 mg/dl or more in men or 6 mg/dl or more in women

    Diagnostic Test: Hyperuricemia

Interventions

  • Diagnostic testHyperuricemia

    Hyperuricemia vs. normouricemia

06

What researchers measure

Primary outcomes

  1. The prevalence of metabolic syndrome

    Based on the Taiwan criteria, metabolic syndrome must fulfill at least three of the five following criteria: 1) waist circumference more than 90 cm in men or more than 80 cm in women; 2) blood pressure of more than 130 / 85 mm Hg or already on anti-hypertensive medication; 3) fasting glucose of 100 mg/dl or more or already on anti-diabetic agents; 4) triglyceride level of 150 mg/dl or more or already on lipid lowering therapy for hypertriglyceridemia; 5) high-density lipoprotein cholesterol of 40 mg/dl or less in men or 50 mg/dl or less in women; the investigators also replaced the criterion of waist circumference by body mass index of 27 kg/m2 in the definition of metabolic syndrome.

    Time frame: 1 day

Secondary outcomes

  1. Left ventricular hypertrophy - Cornell voltage criteria.

    Left ventricular hypertrophy is defined by Cornell voltage criteria.

    Time frame: 1 day

  2. Left ventricular hypertrophy - Cornell voltage product.

    Left ventricular hypertrophy is defined by Cornell voltage product.

    Time frame: 1 day

  3. Left ventricular hypertrophy - Sokolow-Lyon criteria.

    Left ventricular hypertrophy is defined by Sokolow-Lyon criteria.

    Time frame: 1 day

  4. Left ventricular hypertrophy - Minnesota Code electrocardiographic classification.

    Left ventricular hypertrophy is defined by Minnesota Code electrocardiographic classification.

    Time frame: 1 day

  5. Left ventricular hypertrophy - composite of Cornell voltage criteria, Cornell voltage product, Sokolow-Lyon criteria, Minnesota Code electrocardiographic classification.

    Any of above left ventricular hypertrophy criteria is counted as left ventricular hypertrophy.

    Time frame: 1 day

  6. brief symptom rating scale-5

    Brief symptom rating scale-5 consisted of five items with a total score of 0 to 20. Each items range from 0 to 4 in score, including difficult in falling asleep, anxiety (feeling tense or high-strung), hostility (feeling easily annoyed or irritated), interpersonal sensitivity (feeling inferior to others), depression (feeling depressed or in a low mood) in the past week. The summation of brief symptom rating scale-5 is further classified as normal (score of \<6), mild mood disorder (score of 6-9), moderate mood disorder (score of 10-14), severe mood disorder (score of \>14). Suicidal attempt is an additional item and the score \>1 is considered as severe mood disorder.

    Time frame: 1 day

07

Study locations

1 of 1 sites recruiting
  • Tri-service General Hospital, songshan branch
    Taipei, Songshan Dist. 105, Taiwan
    Recruiting
    • Liu, MD · Contactissac700319@gmail.com · +886-910682383
    • Cheng-Wei Liu, MD · Principal investigator
    • Wei-Cheng Chang, MD · Sub investigator
08

References and documents

Publications

  • Tu CM, Wei TE, Tseng GS, Chen CC, Liu CW. Serum uric acid is associated with incident metabolic syndrome independent of body shape index and body roundness index in healthy individuals. Nutr Metab Cardiovasc Dis. 2021 Oct 28;31(11):3142-3151. doi: 10.1016/j.numecd.2021.07.008. Epub 2021 Jul 24. PubMed 34518090 ↗
  • Liu CW, Ke SR, Tseng GS, Wu YW, Hwang JJ. Elevated serum uric acid is associated with incident hypertension in the health according to various contemporary blood pressure guidelines. Nutr Metab Cardiovasc Dis. 2021 Apr 9;31(4):1209-1218. doi: 10.1016/j.numecd.2021.01.003. Epub 2021 Jan 12. PubMed 33618920 ↗
  • Liu CW, Chen KH, Tseng CK, Chang WC, Wu YW, Hwang JJ. The dose-response effects of uric acid on the prevalence of metabolic syndrome and electrocardiographic left ventricular hypertrophy in healthy individuals. Nutr Metab Cardiovasc Dis. 2019 Jan;29(1):30-38. doi: 10.1016/j.numecd.2018.10.001. Epub 2018 Oct 16. PubMed 30545672 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Mar 2018 (actual). Primary completion is estimated for Dec 2020, 33 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 15, 2018
First posted
Mar 22, 2018
StartActual
Mar 26, 2018
Primary completionEst.
Dec 2020
CompletionEst.
Dec 2020
Last update
Jun 9, 2020
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 9, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03473951
Lead sponsor
National Defense Medical Center, Taiwan
Responsible party
Cheng-Wei Liu (Cardiologist, National Defense Medical Center, Taiwan) — Principal investigator
First posted
Mar 22, 2018
Start date
Mar 26, 2018
Primary completion
Dec 2020 (estimated)
Completion
Dec 2020 (estimated)
Last update
Jun 9, 2020

Study contacts

Liu
Contact
issac700319@gmail.com
+886-2-27642151 ext. 671401

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2020. You cannot join it, but the record below documents what was studied.

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