Post-operative pain relief after vitreo-retinal surgery with Subtenon L Bupivacaine infiltration
| ISRCTN | ISRCTN43292522 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN43292522 |
| Secondary identifying numbers | N0064131841 |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 19/09/2017
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Surgery
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Mr Y K Ghosh
Scientific
Scientific
Academic Unit of Ophthalmology
Birmingham and Midland Eye Centre
City Hospital
Dudley Road
Birmingham
B18 7HQ
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 |
| Scientific title | Post-operative pain relief after vitreo-retinal surgery with Subtenon L Bupivacaine infiltration: a randomised controlled trial |
| Study objectives | Does Subtenon L Bupivacaine significantly reduce requirements for post-operative analgesia after vitreo retinal surgery compared with current analgesia? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Surgery: Analgesia |
| Intervention | Subtenon L Bupivacaine vs current analgesia |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Applicable |
| Drug / device / biological / vaccine name(s) | Subtenon L Bupivacaine |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/11/2003 |
| Completion date | 01/04/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Both |
| Target number of participants | 60 patients |
| Key inclusion criteria | Not provided at time of registration |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/11/2003 |
| Date of final enrolment | 01/04/2004 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Academic Unit of Ophthalmology
Birmingham
B18 7HQ
United Kingdom
B18 7HQ
United Kingdom
Sponsor information
Department of Health
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.dh.gov.uk/Home/fs/en |
|---|
Funders
Funder type
Government
Sandwell and West Birmingham Hospitals NHS 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 |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results | 01/02/2005 | Yes | No |
Editorial Notes
HF 19/09/2017: corrected pub stage.
