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Comparison of three diagnostic tools for latent tuberculosis in haemodialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN52111135
Enrollment
162
Registered
2008-03-26
Start date
2008-03-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Latent tuberculosis Infections and Infestations Tuberculosis

Interventions

Agreement of three diagnostic tests for latent tuberculosis will be tested in haemodialysis patients. Blood samples are taken for: 1. Quantiferon-gold assay, an enzyme linked immunosorbent assay (ELIS

Sponsors

Gachon University of Medicine and Science (South Korea)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Chronic maintenance haemodialysis patients who continue to receive haemodialysis for more than three months in the Gil Medical Centre 2. Older than 18 years, and less than 80 years, either sex 3. Agrees to participate in this trial 4. Medical staff in the haemodialysis centre of the Gil Medical Centre

Exclusion criteria

Exclusion criteria: 1. Patients who suffer from skin diseases which may interfere with Mantoux test 2. Patients with an active infection, except tuberculosis 3. Patients who cannot make independent decision due to mental disorders

Design outcomes

Primary

MeasureTime frame
1. Skin test: positive or negative 2. Quantiferon-gold: positive or negative 3. T-spot test: positive or negative These outcomes will be measured on the day of testing.

Secondary

MeasureTime frame
1. Skin test: size of induration 2. Quantiferon-gold: concentration 3. T-spot test: number, mean area These outcomes will be measured on the day of testing.

Countries

Korea, South

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026