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Lidocaine: Effect of Lidocaine in Chronic Cough

Effect of Lidocaine and Its Delivery in Patients With Chronic Cough

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01252225
Enrollment
30
Registered
2010-12-02
Start date
2011-02-28
Completion date
2011-05-31
Last updated
2011-09-16

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

Conditions

Chronic Cough

Keywords

Chronic Cough, Lidocaine

Brief summary

People cough in order to clear their airways. Most coughs are caused by viruses and settle down by themselves, but some people develop persistent coughing which can be anywhere from 8 weeks to several years. This is called chronic cough. People with chronic cough find the symptom distressing and it can have a major impact on their quality of life. Patients with chronic cough often report a sensation at the back of their throat which makes them feel an urge to cough. There is some evidence that Lidocaine (an anaesthetic used during medical procedures) can suppress a person's cough when given to patients via a nebuliser (a machine that turns liquid into a fine mist). It is currently unknown whether using a local anaesthetic, such as Lidocaine, in the form of a throat spray would successfully suppress a person's cough. A throat spray would be an easier treatment option in chronic cough patients. Thus, the investigators research aims to compare cough rates, severity and urge to cough scores between Lidocaine throat spray and nebulised Lidocaine.

Interventions

DRUG10 % Lidocaine

600 mg Nebulised Lidocaine ( 6 mls of 10 % Lidocaine) one-off dose

DRUG0.9% saline

6 mls of 0.9% saline nebulised followed by 1 ml of 0.9% saline as throat spray

Sponsors

Manchester University NHS Foundation Trust
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male and female subjects, age 18 years and over. * History of cough for more than 8 weeks. * Normal chest x ray * Chronic idiopathic cough or chronic cough resistant to treatment of specific triggers.

Exclusion criteria

* Smoking status: * Current smokers * Ex smokers with history of smoking \> 20 pack years or those who have given up \< 6 months ago. * Prohibited medications: * Use of medications likely to suppress / affect cough including codeine, morphine, pregabalin, gabapentin, amitriptylline, angiotensin converting enzyme inhibitors (type 1) and baclofen. * Use of any anti-arrhythmic medication. * Use of cimetidine, beta blockers, or diuretics. * Cardiovascular conditions: * Sinoatrial disease, bradycardia or all types of heart blocks. * History of ischaemic heart disease or heart failure. * Clinically significant abnormal electrocardiogram (ECG) at Screening or Baseline. * History of cardiac surgery * Respiratory conditions: o Asthma. * Central nervous system / Peripheral nervous system conditions: * Epilepsy. * Myasthenia gravis. * Miscellaneous: * History of hepatic or renal dysfunction. * Porphyria * History of hypersensitivity to Lidocaine or related drugs. * Pregnancy or breast feeding. * Participation in another trial within the preceding 6 weeks. * Trauma or ulceration to oral mucosa. * History of chest or upper airway infection within the past 6 weeks. * Conditions which may affect cough response such as stroke, diabetes, Parkinson's Disease.

Design outcomes

Primary

MeasureTime frameDescription
Objective cough counts over 10 hours post dose. Change in Urge to cough and Visual Analogue Score (VAS).over 24 hours following treatmentpatients will wear a cough recorder device for a 24 hour period. The recordings will then be analysed to reveal how many times the patient coughed.

Secondary

MeasureTime frameDescription
Heart rateover 2 hoursto document any change in heart rate after treatment
Mouth Numbnessover 24 hours following treatmentDuration of mouth numbness will be subjectively assessed by asking patients about the presence of mouth numbness and its duration after treatment.
Electrocardiogram (ECG)15 minutes after treatmentECG will be recorded before treatment and 15 minutes after treatment to rule out any arrhythmias

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026