The effect of timing of the application of topical anaesthetic prior to rigid nasendoscopy
| ISRCTN | ISRCTN40986271 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN40986271 |
| Protocol serial number | N0212177261 |
| Sponsor | Record Provided by the NHSTCT Register - 2006 Update - Department of Health |
| Funder | Royal United Hospital Bath NHS Trust |
- Submission date
- 29/09/2006
- Registration date
- 29/09/2006
- Last edited
- 08/12/2010
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Mr David Pothier
Scientific
Scientific
ENT
Royal United Hospital
B&NES
Bath
BA1 3NG
United Kingdom
| Phone | +44 (0)1225 428331 |
|---|---|
| David.Pothier@ruh-bath.swest.nhs.uk |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Is it best to wait one or ten minutes before performing nasendoscopy after the application of cophenylcaine? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Nasendoscopy |
| Intervention | Quantitative, randomised controlled trial Treatment 1: wait 1 minute Treatment 2: wait 10 minutes |
| Intervention type | Procedure/Surgery |
| Primary outcome measure(s) | Visual analogue scales of pain and discomfort for patients. |
| Key secondary outcome measure(s) | Not provided at time of registration |
| Completion date | 01/09/2006 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 50 |
| Key inclusion criteria | Patients who, by the decision of the examining clinician, need to undergo examination of their nasal cavity using rigid nasendoscopy. |
| Key exclusion criteria | 1. Unable to provide informed consent 2. Patients in whom lignocaine or phenylphrine is contra indicated for medical reasons 3. Patients in whom only one nasal cavity or part of one cavity is to be examined |
| Date of first enrolment | 01/03/2006 |
| Date of final enrolment | 01/09/2006 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
ENT
Bath
BA1 3NG
United Kingdom
BA1 3NG
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 |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results | 01/03/2007 | Yes | No |
