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 |
| Protocol serial number | N0190137106 |
| Sponsor | Department of Health |
| Funder | Queen Victoria Hospital NHS Trust (UK) |
- 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
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| 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(s) |
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. |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 30/07/2006 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 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
- United Kingdom
- England
Study participating centre
The Queen Victoria Hospital NHS Trust
East Grinstead
RH19 3DZ
United Kingdom
RH19 3DZ
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
