Skip to content

Study for latent tuberculosis infection intervention among close contacts of pulmanary tuberculosis patients

Study for latent tuberculosis infection intervention among close contacts of pulmanary tuberculosis patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019658
Enrollment
Unknown
Registered
2018-11-21
Start date
2018-12-01
Completion date
Unknown
Last updated
2018-11-26

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

Conditions

Tuberculosis

Interventions

Intervention group A:Drug A: Isoniazid, adults: Weight=50kg, 600mg, weight=50kg, 500mg
Children: no more than 300mg(10~15mg/kg), twice weekly for 24 doses.Drug B: Rifapentine, adults: Weight=50kg, 600mg, weight=50kg, 450mg
Children aged more than 5: 10~20mg/Kg, no more than 450mg, twice weekly for 24 doses.
Intervention group B:Isoniazid, Daily for 180 doses.Dosage: adults: 300mg/dose, children: no more than 300mg/dose(10mg/kg).
Not taking medicine group C (Not taking medicine for any reason):No interventons

Sponsors

Chinese center for disease control and prevention
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Local household registration or resident population; 2. aged between 5-65 years; 3. Signed voluntarily informed consent.

Exclusion criteria

Exclusion criteria: 1. Previous and current tuberculosis patients; 2. Index case is rifampicin and/or isoniazid-resistant tuberculosis; 3. Pregnant or lactating or preparing for pregnancy; 4. Alcohol/drug addicts; 5. Mental disorders, deaf/mute disabled who can not cooperate with the study; 6. HIV-infected or AIDS; 7. HCV infection; 8. A history of treatment for > 14 consecutive days with a rifapentine or > 30 consecutive days with INH at any time during the 2 years prior to enrollment; 9. Contraindications for taking isoniazid including abnormal liver function, mental disorder patients, patients with epilepsy; 10. Contraindications for taking rifapentine/rifampin: those who are allergic to rifampicin/rifamycin-based antibacterials, severe abnormal liver function, biliary obstruction, and pregnant women; 11. Liver disease (ALT or AST > two times normal limit, or total bilirubin > 1.5 times normal limit, or/and with clinical evidence of hepatic damage; 12. Renal inadequacy or diminished; 13. White blood count (WBC) < 2.0×10^9/L; 14: Past Cirrhosis; 15. Past epilepsy; 16. Others.

Design outcomes

Primary

MeasureTime frame
Advent of active pulmonary tuberculosis;

Countries

China

Contacts

Public ContactZhang Hui

Chinese center for disease control and prevention

zhanghui@chinacdc.cn+86 010-58900514

Outcome results

None listed

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