Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
NCT07488598

Efficacy of Behavioral Therapy for Chronic Refractory Cough

Led by Assiut University · Updated on 2026-04-23

30

Participants Needed

1

Research Sites

60 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic cough is defined as cough persisting for more than eight weeks. It is a common clinical problem that significantly impairs patients' physical, psychological, and social quality of life. Chronic cough remains a diagnostic and therapeutic challenge despite systematic evaluation and treatment of common etiologies such as asthma, gastroesophageal reflux disease

CONDITIONS

Official Title

Efficacy of Behavioral Therapy for Chronic Refractory Cough

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years and older with a normal chest radiograph
  • Chronic cough lasting more than eight weeks that does not respond to standard treatments for asthma or gastroesophageal reflux disease
  • Clinical signs of laryngeal hyperresponsiveness, including cough triggered by talking, laughing, cold air, or irritants, along with symptoms like throat irritation, voice changes, or frequent throat clearing
Not Eligible

You will not qualify if you...

  • Current smokers or those who quit within the last six months
  • Evidence of active lung or heart disease, recent respiratory infection, or recent use of angiotensin-converting enzyme inhibitors
  • Significant structural problems of the larynx, neurological conditions affecting cough control, or inability to follow study procedures
  • Head and neck issues such as sinusitis, glottal insufficiency, or primary muscle tension dysphonia

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

Assuit University hospitals

Asyut, Egypt

Actively Recruiting

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Research Team

M

Mohamed Shaaban Mohamed Mahfouz, Resident

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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