Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 60Years
All Genders
NCT07103980

Inhaled Mesenchymal Stem Cell-Derived Exosomes in the Treatment of Post-Infectious Cough: A Single-Center Randomized Controlled Clinical Trial

Led by Shanghai Changzheng Hospital · Updated on 2025-08-05

40

Participants Needed

1

Research Sites

76 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is an exploratory clinical trial. It is intended to investigate the efficacy of mesenchymal stem cell-derived exosome nebulization in the treatment of postinfectious cough through a randomized controlled clinical study, with a view to providing better treatment options for patients with postinfectious cough, improving their quality of life, and providing reference data for the subsequent multi-center clinical trials.

CONDITIONS

Official Title

Inhaled Mesenchymal Stem Cell-Derived Exosomes in the Treatment of Post-Infectious Cough: A Single-Center Randomized Controlled Clinical Trial

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18-60 years
  • Diagnosis of post-infectious cough with symptoms lasting 3 to 8 weeks after acute respiratory infection has resolved
  • Chest X-rays are normal
  • Cough is dry or with small amounts of mucoid phlegm
  • Baseline cough visual analog scale score of 60 mm or higher
Not Eligible

You will not qualify if you...

  • Presence of other causes of cough such as upper airway cough syndrome, eosinophilic bronchitis, gastroesophageal reflux cough, bronchial asthma, COPD, or bronchiectasis
  • Serious lung diseases like lung cancer, tuberculosis, or pulmonary fibrosis
  • Serious comorbid conditions including cardiovascular, cerebrovascular, liver, kidney, or hematopoietic system diseases
  • Current or former smokers who quit less than 6 months ago
  • Body temperature of 37.3°C or higher
  • Elevated white blood cell or neutrophil count above normal limits
  • Abnormal chest X-rays
  • History or suspicion of alcohol or drug abuse or mental illness
  • Pregnancy, lactation, or planning pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shanghai changzheng hospital

Shanghai, Shanghai Municipality, China, 200000

Actively Recruiting

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Research Team

H

Hao Tang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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