Ultrasound versus abrasive scrubbing in contaminated facial wounds - a pilot study
| ISRCTN | ISRCTN92375603 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN92375603 |
| Secondary identifying numbers | N0544103910 |
- Submission date
- 12/09/2003
- Registration date
- 12/09/2003
- Last edited
- 05/02/2018
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Injury, Occupational Diseases, Poisoning
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
Mr Leo H-H Cheng
Scientific
Scientific
Clinic 8
Box 47
Department of Oral and Maxillofacial Surgey
Addenbrooke's Hospital
Cambridge
CB2 2QQ
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 |
| Participant information sheet | Not available in web format, please use the contact details to request a patient information sheet |
| Scientific title | Ultrasound versus abrasive scrubbing in contaminated facial wounds - a pilot study |
| Study objectives | Pilot study of contaminated facial wound debridement |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Skin and Connective Tissue Diseases: Facial wounds |
| Intervention | Pilot study. Single-blind, randomised controlled trial to assess debridement of contaminated facial wounds using a Piezon Ultrasonic Scaler compared to abrasive scrubbing. Subjects are treated under General Anaesthetic for debridement of facial wounds. Standard photographs of wounds will be taken immediately pre- and postoperatively, then at 5 days review and 2 months review. A blinded examiner will assess wound healing and the photographs graded on a scale of 1-6 (poor-excellent debridement). |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 14/09/2001 |
| Completion date | 05/03/2003 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 30 |
| Key inclusion criteria | 30 patients |
| Key exclusion criteria | Does not meet inclusion criteria |
| Date of first enrolment | 14/09/2001 |
| Date of final enrolment | 05/03/2003 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Addenbrooke's Hospital
Cambridge
CB2 2QQ
United Kingdom
CB2 2QQ
United Kingdom
Sponsor information
Department of Health (UK)
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.doh.gov.uk |
|---|
Funders
Funder type
Other
Cambridge Consortium - Addenbrookes (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 |
Editorial Notes
05/02/2018: No publications found, verifying study status with principal investigator.
