Skip to content

Diffuse noxious inhibitory controls in chronic cough

Diffuse Noxious Inhibitory Controls in chronic cough: a randomised, four-way cross-over study of 20 healthy subjects and 20 patients with chronic cough

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN31901405
Enrollment
40
Registered
2011-04-07
Start date
2011-01-04
Completion date
Unknown
Last updated
2017-02-27

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

Conditions

Chronic cough Respiratory Chronic cough

Interventions

Basal conditions: During both blocks of capsaicin inhalation (block 1 and block 2) participants will not place their hand in a water bath and will be instructed to cough freely. Control conditions:

Sponsors

University Hospitals of South Manchester NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy volunteers: 1. Aged over 18 years old, either sex 2. Normal lung function 3. No current or past history of chronic cough or chronic respiratory illness 4. No current or past history of chronic pain, irritable bowel syndrome or chronic headaches 5. No current or past history of psychiatric illness 6. No current history of reflux disease or post-nasal drip syndrome Chronic cough patients: 1. Aged over 18 years old, either sex 2. Chronic cough, defined as a cough lasting longer than 8 weeks despite investigation and/or treatment trials for cough variant asthma, post-nasal drip and gastro-oesophageal reflux disease 3. Normal chest x-ray 4. Normal lung function 5. Can safely omit long-acting bronchodilators (if taking)

Exclusion criteria

Exclusion criteria: 1. Recent upper respiratory tract infection (less than 4 weeks) 2. Pregnancy or breastfeeding 3. Use of angiotensin converting enzyme (ACE) inhibitors 4. Any centrally acting medication which could alter the sensitivity of the cough reflex 5. History of drug or alcohol abuse 6. Current smoker or ex-smoker with greater than 10 pack year smoking history

Design outcomes

Primary

MeasureTime frame
Effect of painful cold water bath on cough response, recorded following each of the four randomised interventions. Each intervention will take place at least 48 hours apart.

Secondary

MeasureTime frame
1. Effect of conscious cough suppression on cough response 2. Comparison of effects by group and gender The primary and secondary outcome measures will be recorded following each of the four randomised interventions. Each intervention will take place at least 48 hours apart.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026