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The clinical investigation of the curative effect about Nai-Lao-Kang combination with antituberculotics in MDR-TB

The clinical investigation of the curative effect about Nai-Lao-Kang combination with antituberculotics in MDR-TB

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034800
Enrollment
Unknown
Registered
2020-07-19
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-07-20

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

Conditions

multidrug resistance tuberculosis

Interventions

Sponsors

Chongqing Zhihui Institute of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients meeting the mdr-ptb/rr-ptb diagnostic criteria; 2. Those who meet the criteria for syndrome differentiation of lung Yin deficiency in traditional Chinese medicine; 3. According to the purpose of the clinical trial and the characteristics of this type of disease, the subjects are between 18 and 65 years old; 4. No obvious abnormalities were found in liver and kidney function, fasting blood glucose and electrocardiogram.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. People with allergic constitution, or who are known to be allergic to any of the drugs (Chinese and western medicine) used in the treatment scheme of this subject; 3. Patients with malignant tumors, pneumoconiosis, epilepsy and autoimmune diseases; 4. Patients with severe primary diseases such as liver, kidney, cardiovascular and cerebrovascular diseases, hematopoietic system and endocrine system;

Design outcomes

Primary

MeasureTime frame
Evaluation of curative effect of TCM syndrome;CT value (lesion repair area);

Secondary

MeasureTime frame
Drug susceptibility to drug-resistant tuberculosis;

Countries

China

Contacts

Public ContactLi QuanTang

Chongqing Hospital of Traditional Chinese Medicine

326809469@qq.com+86 18680805765

Outcome results

None listed

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