The effect of timing of the application of topical anaesthetic prior to rigid nasendoscopy
| ISRCTN | ISRCTN40986271 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN40986271 |
| Secondary identifying numbers | N0212177261 |
- 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
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
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Not specified |
| Study type | Not Specified |
| Scientific title | |
| Study hypothesis | 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 |
| Condition | Nasendoscopy |
| Intervention | Quantitative, randomised controlled trial Treatment 1: wait 1 minute Treatment 2: wait 10 minutes |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Visual analogue scales of pain and discomfort for patients. |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/03/2006 |
| Overall study end date | 01/09/2006 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 50 |
| Participant inclusion criteria | Patients who, by the decision of the examining clinician, need to undergo examination of their nasal cavity using rigid nasendoscopy. |
| Participant 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 |
| Recruitment start date | 01/03/2006 |
| Recruitment end date | 01/09/2006 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
ENT
Bath
BA1 3NG
United Kingdom
BA1 3NG
United Kingdom
Sponsor information
Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Government
Government
The Department of Health, Richmond House, 79 Whitehall
London
SW1A 2NL
United Kingdom
| Phone | +44 (0)20 7307 2622 |
|---|---|
| dhmail@doh.gsi.org.uk | |
| Website | http://www.dh.gov.uk/Home/fs/en |
Funders
Funder type
Government
Royal United Hospital Bath NHS Trust
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 |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results | 01/03/2007 | Yes | No |
