The use of topical antibacterial skin ointment (TASO) in the management of soft tissue wounds: A randomised controlled trial
| ISRCTN | ISRCTN39666702 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN39666702 |
| Protocol serial number | N0186150989 |
| Sponsor | Department of Health |
| Funder | Poole Hospital NHS Trust (UK) |
- Submission date
- 30/09/2005
- Registration date
- 30/09/2005
- Last edited
- 08/04/2014
- 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 Michael Bater
Scientific
Scientific
Maxillofacial Department
Poole Hospital NHS Trust
Longfleet Road
Poole
BH15 2JB
United Kingdom
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | Is there any improvement in wound healing or cosmesis by prescription of topical ointments following suture of soft tissue wounds? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Injury, Occupational Diseases, Poisoning: Wound healing |
| Intervention | Antibacterial ointment (TASO) vs placebo vs no ointment - A randomised controlled trial |
| Intervention type | Other |
| Primary outcome measure(s) |
At review for suture removal the wounds would be assessed for healing. At a subsequent review, the wound would be assessed for cosmesis. The groups would be compared and the best treatment modality ascertained. |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 30/04/2005 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Key inclusion criteria | Patients with facial lacerations requiring suture |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 30/04/2004 |
| Date of final enrolment | 30/04/2005 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Maxillofacial Department
Poole
BH15 2JB
United Kingdom
BH15 2JB
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 |