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CompletedNCT02572466Updated Jan 29, 2016

Study of High Sensitive Troponin-I Level in End-stage Renal Disease Patients Receiving Hemodialysis

An observational study in End-stage Renal Disease, sponsored by Chulalongkorn University. Completed at 1 site in Thailand. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-01-29.

Sponsored by Chulalongkorn University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
207
Ages
18 Years and older
Sex
All
01

Study summary

This study objective is to compare the high sensitive troponin-I level in end-stage renal disease patients received hemodialysis without acute cardiovascular event with healthy population. The investigators also determine the effect of hemodialysis on troponin I level as the secondary objective.

Read the detailed description

Human cardiac Troponin I (cTnI) is an composition of Troponin which is found in heart muscle cells. Molecular weight of cTnI is 23,875 Dalton consisting of 209 amino acids. [1,2] The cTnI have been used in the diagnosis of acute myocardial infarction(AMI). [3,4,5] According to ESC / ACCF / AHA / WHF, diagnosis of acute myocardial infarction rely on the data from clinical symptoms, Electrocardiogram (EKG) changes in the specific pattern, such as ST-segment elevation / depression, new left bundle branch block, and cardiac biomarker level rise over the 99th percentile upper reference limit, which makes the cTnI level was used to help in making diagnosis for patient coming with symptoms of angina in emergency room.

The current cTnI detecting test has developed more and more high sensitive(called "high-sensitive troponin-I; hsTnI") which can detected in the range 10-50,000 pg / ml (ng / L) [6], and it can detected cTnI level even in normal people unlike cTnI, which only reported positive or negative or lower than the limit of detection. Due to ARCHITECT stat High sensitive Troponin-I (Abbott diagnostic) capabilities, hsTnI level can be detected in normal people up to 96 percent.[7] The reference range of hsTnI which has been researched by Apple FS, et al.(2012) studying the 19 types of cardiac troponin I and T measurement was established. The 99th percentile values for general healthy population without hypertension, diabetes, kidney disease and myocardial infarction, aged 18-64 years was 36 ng / L in men (N = 272), 15 ng / L in women (N = 252) [7].

However, research to find the reference of hsTnI in some groups , especially in patients with kidney disease is still limited and the diagnosis of acute myocardial infarction also use the 99th percentile as the reference source which was researched in healthy population[7] which makes it difficult to interpret. Sometimes doctors may concluded that patients with rising hsTnI because of kidney disease. According to the research in the next section, there are both support and against in this idea. Therefore, the researchers aim to study hsTnI in patients with end-stage renal disease received hemodialysis compare with normal population.

02

Conditions studied

  • End-stage Renal Disease

Keywords

  • high-sensitive troponin-I
  • End-stage renal disease
  • hemodialysis
03

In context

Kidney Diseases

3,840 studies on the registry are indexed under Kidney Diseases; 500 are open to participants now.

This study's enrollment of 207 is close to the median of 192 across 1,033 observational studies indexed under Kidney Diseases.

Browse Kidney Diseases studies →

Lead sponsor

Chulalongkorn University is the lead sponsor of 312 studies on the registry; 59 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

ESRD group End-stage renal disease patients receiving regular hemodialysis at King Chulalongkorn memorial hospital, Bhumirajanagarindra kidney institute hospital.

Control group Patients who come to OPD at King Chulalongkorn memorial hospital for their follow up blood check.

Inclusion criteria

  • Aged 18 years or more.
  • was diagnosed as End-stage renal disease for more than one year.
  • Attend hemodialysis 3 times a week consistently for more than 6 months.
  • Hemodialysis with Kt/V > 1.2
  • No urine output or is less than 500 ml per day.
  • No symptoms of myocardial infarction Or were hospitalized with the similar diagnosis during the two weeks.

Exclusion criteria

Exclusion Criteria:

  • Could not complete hemodialysis, or Kt / V \<1.2
  • Has symptoms of myocardial infarction while receiving dialysis
  • Has the abnormal symptom (fever, chill, low BP) While receiving dialys
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
207 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • ESRD group

    1. Aged 18 years or older. 2. was diagnosed as End-stage renal disease for more than one year. 3. Attend hemodialysis 3 times a week consistently for more than 6 months. 4. Hemodialysis with Kt/V \> 1.2 5. No urine output or is less than 500 ml per day. 6. No symptoms of myocardial infarction Or were hospitalized with the similar diagnosis during the two weeks.

    Other: Hemodialysis

  • Control group

    1. Aged 18 years or older. 2. without kidney disease (eGFR \> 60 ml/min/1.73m2)

Interventions

  • OtherHemodialysis

    ESRD group received long-term hemodialysis

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What researchers measure

Primary outcomes

  1. High Sensitive Troponin-I in ESRD group vs Control group

    ESRD group * Measure the High Sensitive Troponin-I level before the hemodialysis session Control group * Measure the High Sensitive Troponin-I as an additional test to their follow up blood check.

    Time frame: 10 months

Secondary outcomes

  1. High Sensitive Troponin-I in pre-hemodialysis vs post-hemodialysis

    Measure the High Sensitive Troponin-I level before the hemodialysis session comparing to the level after the hemodialysis session.

    Time frame: 4 hours

07

Study locations

1 site
  • King Chulalongkorn Memorial Hospital
    Bangkok, 10330, Thailand
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 29, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02572466
Lead sponsor
Chulalongkorn University
Responsible party
Khajohn Tiranathanagul (Assistant Professor, Chulalongkorn University) — Principal investigator
First posted
Oct 9, 2015
Start date
Feb 2015
Primary completion
Nov 2015
Completion
Nov 2015
Last update
Jan 29, 2016

Study contacts

Khajohn Tiranathanagul, MD
principal investigator · Chulalongkorn University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2016. You cannot join it, but the record below documents what was studied.

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