Skip to content

Comparison of the Efficacy and Safety of Mirogabalin versus Gabapentin in the Treatment of Refractory Chronic Cough: A Single-Center, Open-Label, Randomized Controlled Trial

Comparison of the Efficacy and Safety of Mirogabalin versus Gabapentin in the Treatment of Refractory Chronic Cough: A Single-Center, Open-Label, Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123743
Enrollment
Unknown
Registered
2026-04-29
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

refractory chronic cough

Interventions

Mirogabalin:Mirogabalin

Sponsors

Tongji Hospital of Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age > 18 years; 2. Cough as the sole or predominant symptom, duration > 8 weeks, with no significant abnormalities on chest CT; 3. Cough Visual Analogue Scale (VAS) score = 40mm; 4. According to the "Guidelines for the Diagnosis and Management of Cough (2021)", chronic cough remains unexplained after recommended standardized investigations and treatment; or chronic cough that persists despite empirical treatment targeting known etiologies of chronic cough; or chronic cough where there is evidence of an etiology but treatment response is poor and cough persists; 5. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Current smokers or those who quit smoking less than 2 years ago; 2. History of respiratory tract infection within the past 8 weeks; 3. Pregnant or lactating women; 4. Use of angiotensin-converting enzyme inhibitors (ACEI) within the past 3 months or requiring long-term ACEI therapy; 5. Contraindication or allergy to the study drugs; 6. Comorbid severe cardiovascular disease, hepatic or renal insufficiency, neurological disorders, mental illness or drug dependence, hearing or communication impairment; 7. Any other condition deemed by the investigator to be unsuitable for trial participation.

Design outcomes

Primary

MeasureTime frame
Cough resolution rate ar 10 week;

Secondary

MeasureTime frame
Hull Airway Reflux Questionnaire (HARQ) score;Leicester Cough Questionnaire (LCQ) score;GerdQ questionnaire score;Capsaicin cough threshold;Cough Evaluation Test (CET) score;Cough Visual Analogue Scale (VAS) score;

Countries

China

Contacts

Public ContactYu Li

Tongji Hospital of Tongji University

96778@tongji.edu.cn+86 13816699078

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026