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Not Yet RecruitingNCT07272278

Prospective Clinical Study on the Clinical Efficacy and Prognostic Outcome of ICS/LABA Combined With Liqin Zhike Formula in the Treatment of Cough Variant Asthma

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
236 (estimated)
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To investigate the impact of the combination of ICS/LABA and Liqin Zhike Formula on the clinical efficacy and prognostic outcomes of cough variant asthma.

Detailed description

A total of 236 patients with cough variant asthma were enrolled and randomly assigned in a 1:1 ratio. Among them, 118 patients were allocated to the Western medicine treatment group and received ICS/LABA + conventional therapy, while the other 118 patients were assigned to the integrated Chinese and Western medicine treatment group and received ICS/LABA + Liqin Zhike Formula. The treatment intervention period for both groups was 2 months, followed by a 12-month drug-discontinuation follow-up. During the 12-month follow-up period, symptom recurrence rate, asthma symptom remission rate, and adverse reactions were observed. The primary study endpoint was the symptom recurrence rate in patients with cough variant asthma during the 12-month follow-up. The secondary study endpoints were the asthma symptom remission rate and adverse reactions.

Conditions

Interventions

TypeNameDescription
DRUGICS+LABACVA patients receive ICS/LABA treatment
DRUGChinese Medicine FormulaCVA patients receive ICS/LABA + Liqin Zhike Formula treatment

Timeline

Start date
2025-12-01
Primary completion
2026-12-30
Completion
2026-12-30
First posted
2025-12-09
Last updated
2025-12-09

Source: ClinicalTrials.gov record NCT07272278. Inclusion in this directory is not an endorsement.