Clinical trial comparing sclerification and non sclerification during nail surgery techniques
| ISRCTN | ISRCTN32331157 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN32331157 |
| Secondary identifying numbers | N0626176968 |
- Submission date
- 29/09/2006
- Registration date
- 29/09/2006
- Last edited
- 06/10/2014
- 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
Ms Susan Walton
Scientific
Scientific
Podiatry Department
Horton Park Centre
Horton Park
Bradford
BD7 3EG
United Kingdom
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Other |
| Study type | Treatment |
| Scientific title | |
| Study objectives | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Surgery: Nails |
| Intervention | When referrals are received by the nail surgery team leader the patient will be selected for one of the two methods of treatment. A sticker will be attached to the patient's notes, green for sclerify and red for no sclerification. An appointment will be sent to the patient including an information pack outlining the research taking place and issues regarding consent. Attached to the patient notes will be a data sheet, for the podiatrist performing the procedure to complete. |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | To identify which technique if any is more beneficial and cost effective. |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/09/2005 |
| Completion date | 30/09/2007 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Lower age limit | 16 Years |
| Sex | Both |
| Target number of participants | 200 |
| Key inclusion criteria | The research will take place at Shipley Health Centre, Horton Park Podiatry Clinic and New Cross Street Podiatry Clinic. The selection criteria will be the existing protocol for a nail surgery patient and aged 16 years and over. The database to administrate the trial will be stored in a secure location. Consent will be obtained prior to participation in the study. |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/09/2005 |
| Date of final enrolment | 30/09/2007 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Podiatry Department
Bradford
BD7 3EG
United Kingdom
BD7 3EG
United Kingdom
Sponsor information
Record Provided by the NHSTCT Register - 2006 Update - Department of Health (UK)
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
Bradford South and West Primary Care 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 |
