Translaryngeal injection of local anaesthetic: a comparison of spread following injection at deep end inspiration with deep end expiration phases of the respiratory cycle
| ISRCTN | ISRCTN45086464 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN45086464 |
| Secondary identifying numbers | N0190137106 |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 06/11/2014
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr P Larcombe
Scientific
Scientific
The Queen Victoria Hospital NHS Trust
Holtye Road
East Grinstead
RH19 3DZ
United Kingdom
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Scientific title | |
| Study objectives | To compare the distribution of spread of local anaesthetic following translaryngeal injection at end inspiration versus end expiration for topicalisation of airway prior to awake fibreoptic nasal intubation. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Surgery: Anaesthesia |
| Intervention | Prospective randomised controlled observational study; pilot study |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Airway reactivity on fibreoptic intubation will be graded and recorded. The blinded research anaesthetist will record a patient discomfort visual analogue score for the procedure on routine follow up. |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 30/04/2004 |
| Completion date | 30/07/2006 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 20 |
| Key inclusion criteria | Adults undergoing awake fibreoptic nasal intubation for scheduled or urgent surgery |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 30/04/2004 |
| Date of final enrolment | 30/07/2006 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
The Queen Victoria Hospital NHS Trust
East Grinstead
RH19 3DZ
United Kingdom
RH19 3DZ
United Kingdom
Sponsor information
Department of Health
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.dh.gov.uk/Home/fs/en |
|---|
Funders
Funder type
Government
Queen Victoria Hospital NHS Trust (UK)
No information available
Results and Publications
| Intention to publish date | |
|---|---|
| Individual participant data (IPD) Intention to share | No |
| IPD sharing plan summary | Not provided at time of registration |
| Publication and dissemination plan | Not provided at time of registration |
| IPD sharing plan |
