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Study identifier: NCT06403943 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy Safety BaiDiZiYin ShenQiYiFei Adjunctive Treatments Pulmonary Tuberculosis

Condition: Adjuvant · Treatment · Tuberculosis  ·  Sponsor: Beijing Chest Hospital

PhasePhase 4
Planned participants292
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

This study is designed to further strengthen the clinical application evidence of BaidiZiyin Pill and ShenqiYifei Pill in the treatment of tuberculosis. To be included in the initial treatment of pulmonary tuberculosis patients, on the basis of standardized Western medicine treatment, BaidiZiyin Pills and ShenqiYifei Pills will be used to evaluate the clinical efficacy and safety of their products. 1. Evaluate the improvement of symptoms in the adjuvant treatment of newly treated pulmonary tuberculosis with BaidiZiyin Pill and ShenqiYifei Pill. 2. Explore the sputum negative conversion time and sputum negative conversion rate of BaidiZiyin Pill and ShenqiYifei Pill as adjunctive treatments for newly treated pulmonary tuberculosis. 3. Explore the protective effects of BaidiZiyin Pill and ShenqiYifei Pill on adverse reactions caused by chemotherapy.

This description comes directly from the study's public registry record.

Talk to the study team

WENJUAN NIE, DR  ·  +86 10 89509331  ·  94642975@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Beijing Chest Hospital affiliated to Capital Medical UniversityBeijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06403943