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 |
| Secondary identifying numbers | N0016173487 |
- 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
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| 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 |
| Pharmaceutical study type(s) | |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Tisseel® glue |
| Primary outcome measure | Independent observer wounds and questionnaire patient |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/01/2004 |
| Completion date | 01/12/2005 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 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
- England
- United Kingdom
Study participating centre
Ophthalmological Surgery
London
W6 8RF
United Kingdom
W6 8RF
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
Hammersmith Hospital NHS Trust (UK)
No information available
NHS R&D Support Funding 2004/05 (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
02/06/2017: No publications found in PubMed, verifying study status with principal investigator
