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Study of the combination of the Tibetan medicine Rhodiola rosea and traditional first-line anti-tuberculosis drugs to improve the clinical prognosis of tuberculosis

Study of the combination of the Tibetan medicine Rhodiola rosea and traditional first-line anti-tuberculosis drugs to improve the clinical prognosis of tuberculosis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071928
Enrollment
Unknown
Registered
2023-05-29
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Infection and immunity

Interventions

Intervention group:On top of the anti-tuberculosis treatment(HRptE/HELfx/HRE), add Rhodiola Rosea injection, 10 mL of Rhodiola Rosea injection (Tonghua Yusheng Pharmaceutical Co., Ltd., State Pharmaco
Control group :Anti-tuberculosis treatment (HRptE/HELfx/HRE)

Sponsors

Shanghai Public Health Clinical Center, Fudan University, Shanghai, People’s Republic of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age 60-80 years; 2) Any gender; 3) Those with a confirmed diagnosis of sensitive tuberculosis; 4) Duration of current anti-tuberculosis treatment less than 2 weeks; 5) Traditional Chinese Medicine (TCM) typology of Yin deficiency and fire type/Qi deficiency type; 6) Patient's compliance and geographical location of residence to meet the need for follow-up; 7) Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1) Persons with severe cardiac, pulmonary, cerebral, renal, gastrointestinal and systemic systemic diseases; 2) Concomitant application of drugs affecting the efficacy observed in this study; 3) Those who are allergic or intolerant to the study drug 4) Those with poor compliance who cannot cooperate; 5) HIV-positive persons; 6) Other subjects who, in the opinion of the investigator, are unable to complete the study as required, or are unsuitable for follow-up participation in the study.

Design outcomes

Primary

MeasureTime frame
Number of immune cell subsets;Cytokines;Sputum cultures;clinical symptoms;

Countries

China

Contacts

Public ContactYan bo

Shanghai Public Health Clinical Center, Fudan University, Shanghai, People’s Republic of China

bo.yan@shphc.org.cn+86 189 3081 3596

Outcome results

None listed

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