drugset / Trial / NCT06901557

Benefits of Jing-Si-Herbal-Tea in Bronchiectasis

NCT06901557 ↗

RandomizedParallel-groupSingle-blindTreatment

Summary

Patients are divided into two groups: the usual care group (UC group) and the Jing-Si Herbal Tea group (JSHT group). * \*\*UC Group\*\*: Receives standard treatment and one placebo packet daily for three months. * \*\*JSHT Group\*\*: Receives standard treatment plus one packet of Jing-Si Herbal Tea daily for three months. Each group includes 30 participants. The study runs from January 1, 2014, to December 31, 2014. Exclusions include severe liver or renal dysfunction and allergy to Jing-Si Herbal Tea. Participants must follow the study protocol. \*\*Assessments\*\*: * \*\*HRQL\*\*: Measured using the COPD Assessment Test (CAT) and the Modified Medical Research Council (mMRC) scale. * \*\*Blood Tests\*\*: Include WBCs, hemoglobin, hematocrit, platelets, BUN, creatinine, uric acid, liver enzymes, electrolytes, CRP, and pPro-BNP. Blood samples will also be analyzed for DAMPs and inflammatory cytokines. * \*\*Pulmonary Function Tests (PFT)\*\*: Conducted with a spirometer per American Thoracic Society guidelines.

Timeline

Start
2024-01-01
Primary completion
2024-12-31
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Jing Si herbal tea Traditional medicine (herbal / TCM) — —

Indications