A randomised comparison of two different methods of intrabronchial lignocaine delivery during flexible bronchoscopy
Completed
- Conditions
- ocal anaesthetic delivery in bronchoscopySurgeryAnaesthesia
- Registration Number
- ISRCTN77331907
- Lead Sponsor
- ancashire Teaching Hospitals NHS Trust (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
All adult patients (either sex) attending Royal Preston Hospital for diagnostic flexible bronchoscopy
Exclusion Criteria
Patients undergoing interventional procedures (e.g. tracheobronchial stenting, transbronchial biopsy or intrluminal palliative therapies)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual analoque scale assessments by doctor, nurse and patient regarding ease of procedure, extent of coughing and patient tolerance. Doctor and nurse questionnaires completed immediately following the procedure. Patient questionnaires completed more than 24 hours later (to ensure there is no lasting effect of any sedative medication used).
- Secondary Outcome Measures
Name Time Method o secondary outcome measures