A randomised prospective study to evaluate blepharoplasty skin closure by Tisseel® glue in comparison with conventional suturing technique
| ISRCTN | ISRCTN55788327 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN55788327 |
| Protocol serial number | N0016173487 |
| Sponsor | Record Provided by the NHSTCT Register - 2006 Update - Department of Health (UK) |
| Funders | Hammersmith Hospital NHS Trust (UK), NHS R&D Support Funding 2004/05 (UK) |
- Submission date
- 29/09/2006
- Registration date
- 29/09/2006
- Last edited
- 02/06/2017
- 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
Miss Jane Olver
Scientific
Scientific
Ophthalmological Surgery
Charing Cross Hospital
Fulham Palace Road
Hammersmith
London
W6 8RF
United Kingdom
| Phone | +44 (0)20 8846 1497 |
|---|---|
| j.olver@imperial.ac.uk |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | A randomised prospective study to evaluate blepharoplasty skin closure by Tisseel® glue in comparison with conventional suturing technique |
| Study objectives | What is the wound characteristics of glue closure in the eyelid? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Suturing techniques |
| Intervention | Patients were randomised between: 1. Tisseel® glue 2. Conventional suturing technique |
| Intervention type | Drug |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Tisseel® glue |
| Primary outcome measure(s) |
Independent observer wounds and questionnaire patient |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 01/12/2005 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 50 |
| Key inclusion criteria | Not provided at time of registration |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/01/2004 |
| Date of final enrolment | 01/12/2005 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Ophthalmological Surgery
London
W6 8RF
United Kingdom
W6 8RF
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 |
Editorial Notes
02/06/2017: No publications found in PubMed, verifying study status with principal investigator
