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A clinical trial of classifciation treatment on multidrug resistant pulmonary tuberculosis

A clinical trial of classifciation treatment on multidrug resistant pulmonary tuberculosis

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-16009380
Enrollment
Unknown
Registered
2016-10-11
Start date
2017-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

multi-drug resistant pulmonary tuberculosis

Interventions

initial treatment faliure of MDR-PTB:thymosin as adjuvant treatment
retreament MDR-PTB:thymosin as adjuvant treatmen

Sponsors

Shanghai Pulmonary Hosptial, Tongji University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients with active pulmonary tuberuclosis, aged 18-65 years old, satisfied with the following conditions will be included: 1. hospitalized patients with active PTB,sputum smear acid fast staining positive or sputume culuture positive, and DST showing at least resistant to isoniazid and rifampin, MDR-PTB; 2. acquired informed consent of hospital ethic commettee and patients who would like to participate in this study.

Exclusion criteria

Exclusion criteria: patients satisfied with any conditions as follows will be exclued from this study: isolation bacterium identified as non-mycobacterium tuberulosis; severe adverse effects against anti-TB drugs, severe liver and renal dysfunction, poor blood gulcose level, complicated by HIV/AIDS, cancer, immune function disorders, pregant and children, elders more than 65 years old.

Design outcomes

Primary

MeasureTime frame
negative rate of sputum culture;

Secondary

MeasureTime frame
lesion obsorption rate;cavity close rate;change of CD3 and CD4;

Countries

China

Contacts

Public ContactFan Lin

Shanghai Pulmonary Hosptial, Tongji University School of Medicine

fanlinsj@163.com+86 13918569516

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 21, 2026