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Completed

NCT Number: NCT07777796

Inhaled vs Intranasal Corticosteroids for Chronic Cough in Upper Airway Cough Syndrome

Chronic cough - a cough lasting eight weeks or longer - is one of the most common reasons people see a lung specialist. It can disturb sleep, make conversation difficult, and reduce quality of life.

In many people, chronic cough occurs together with nose and sinus symptoms such as a blocked or runny nose, mucus dripping down the back of the throat, facial pain, or a reduced sense of smell. This combination is often called upper airway cough syndrome. Doctors commonly treat it with a steroid medicine given either as an inhaler breathed into the lungs or as a spray into the nose. Both are approved, widely used medicines, and treatment guidelines mention both. However, no study has directly compared the two to see whether one relieves cough better than the other, so doctors have little evidence to guide the choice.

This study compares the two treatments directly in adults who have chronic cough together with nose or sinus symptoms. Participants are assigned by chance, like flipping a coin, to one of two groups:

an inhaled steroid (budesonide), breathed in twice a day, or a steroid nasal spray (mometasone furoate), sprayed into each nostril twice a day.

Participants use their assigned treatment for 4 weeks and then return to the clinic. At each visit they rate how severe their cough is by marking a line on a 100-millimetre scale, and they fill in a questionnaire about how the cough affects their daily life.

Participants whose cough has cleared up after 4 weeks finish the study at that point. Those whose cough has not cleared up continue for another 4 weeks: people in the inhaler group carry on with the same inhaler, while people in the nasal spray group continue the spray and also start the inhaler. Everyone who continues returns for a final visit at 8 weeks.

The main question is whether the inhaled steroid reduces cough severity more than the nasal spray after 4 weeks of treatment. The study also looks at cough-related quality of life, and at what happens after treatment is adjusted at 4 weeks.

The study takes place at a single outpatient lung clinic in Katowice, Poland. Both medicines are given at their usual approved doses, and participants are otherwise cared for as in routine practice.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Leszek Giec Upper-Silesian Medical Centre of the Medical University of Silesia

Katowice, Silesian Voivodeship, 40-635, Poland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with chronic cough and signs of chronic upper airway disease

Exclusion criteria

  • Symptoms of an acute respiratory tract infection within 4 weeks prior to enrolment.
  • Diagnosis of any active chronic respiratory disease.
  • Diagnosis of other cause of chronic cough.
  • Use of corticosteroids (oral, intranasal, inhaled, intravenous) within 3 months prior to enrolment.
  • Chronic use of angiotensin-converting enzyme (ACE) inhibitors within 1 month prior to enrolment.
  • Smoking of tobacco products within 6 months prior to enrolment
  • Pregnancy.

Treatment and study plan

Budesonide (400μg/d)

Drug

Inhaled budesonide 400 µg per dose, two doses twice daily (800 µg per administration; 1600 µg total daily), administered by inhaler. In the inhaled corticosteroid arm it is given from randomization as monotherapy for 4 weeks, and continued unchanged at the same dose for a further 4 weeks in participants who have not achieved cough resolution. In the intranasal corticosteroid arm it is added to ongoing intranasal mometasone furoate at week 4 in participants who have not achieved cough resolution, and given for 4 weeks. Maximum total duration of exposure is 8 weeks.

Mometasone Furoate 50mcg Nasal Spray

Drug

Intranasal mometasone furoate 50 µg per dose, two doses into each nostril twice daily (100 µg per nostril per administration; 400 µg total daily), administered by nasal spray. Given from randomization for 4 weeks. Participants who have not achieved cough resolution at 4 weeks continue it at the same dose for a further 4 weeks with inhaled budesonide added. Maximum total duration of exposure is 8 weeks.

Primary outcomes

  1. Change from baseline in cough severity measured by Visual Analog Scale (VAS) at 4 weeks

    Time frame: After 4 weeks of treatment

    Cough severity is self-rated by the participant on a 100-mm visual analog scale ranging from 0 mm ("no cough") to 100 mm ("worst cough"); higher scores indicate more severe cough. The 4-week score is compared between arms by analysis of covariance with the baseline VAS score as covariate, and reported as an adjusted between-group difference with a 95% confidence interval.

Secondary outcomes

  1. Change from baseline in cough severity measured by Visual Analog Scale (VAS) at 8 weeks

    Time frame: After 8 weeks of treatment

    Cough severity self-rated on the 100-mm VAS (0 mm = no cough, 100 mm = worst cough; higher scores indicate more severe cough), analysed by the same ANCOVA model as the primary outcome.

  2. Change from baseline in cough-related quality of life measured by Leicester Cough Questionnaire (LCQ) total score

    Time frame: Baseline, 4 weeks and 8 weeks

    The LCQ is a 19-item self-completed questionnaire assessing the impact of cough over the previous 2 weeks across three domains (physical, psychological, social). Each item is scored 1 to 7; the total score is the sum of the three domain means and ranges from 3 to 21, with higher scores indicating better cough-related quality of life. An improvement of 1.3 points is the published minimal important difference.

  3. Proportion of participants achieving therapeutic success

    Time frame: 4 weeks and 8 weeks

    Therapeutic success is defined as a reduction from baseline of 30 mm or more on the 100-mm cough severity VAS, corresponding to the published minimal clinically important difference. Compared between arms with Fisher's exact test and reported as a risk difference with a 95% confidence interval. Exploratory.

  4. Proportion of participants achieving cough resolution

    Time frame: 4 weeks and 8 weeks

    Cough resolution is defined as a cough severity VAS score of 10 mm or lower. Participants meeting this threshold at 4 weeks complete the study at that visit. Compared between arms with Fisher's exact test and reported as a risk difference with a 95% confidence interval. Exploratory.

  5. Change from baseline in Leicester Cough Questionnaire (LCQ) domain scores

    Time frame: Baseline, 4 weeks and 8 weeks

    LCQ physical (8 items), psychological (7 items) and social (4 items) domain scores, each expressed as the mean of its constituent items on a 1 to 7 scale, with higher scores indicating better cough-related quality of life. Published minimal important differences are 0.8 (physical), 0.9 (psychological) and 0.8 (social).

Sponsors and collaborators

Lead sponsor

Silesian University of Medicine

Other

Registry information

Official study title

Comparison of the Efficacy of Two Therapeutic Regimens in Patients With Chronic Cough With Signs of Rhinitis or Paranasal Sinusitis

Important dates

Study start
2022
Primary completion
2026
Study completion
2026
First posted
Aug 20, 2026
Registry last updated
Aug 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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