Study of timing of ankle block versus inflation of thigh tourniquet in forefoot surgeries
| ISRCTN | ISRCTN42115327 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN42115327 |
| Secondary identifying numbers | N0155182857 |
- Submission date
- 28/09/2007
- Registration date
- 28/09/2007
- Last edited
- 24/10/2016
- 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
Mr M Sundar
Scientific
Scientific
J Block
Royal Oldham Hospital
Rochdale Road
Oldham
OL1 2JH
United Kingdom
| Phone | +44 (0)161 624 0420 |
|---|---|
| manthravadi.sundar@pat.nhs.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 | Study of timing of ankle block versus inflation of thigh tourniquet in forefoot surgeries |
| Study objectives | Is there any difference between timing of inflation of thigh tourniquet and ankle block on post-operative analgesia? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Forefoot |
| Intervention | Randomised controlled trial. Ankle block before inflation of tourniquet or ankle block after inflation of tourniquet. |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Amount of post operative analgesia required: time to first pain perception and amount of analgesia in first 24 hours. |
| Secondary outcome measures | Visual analogue scores for pain. |
| Overall study start date | 01/06/2006 |
| Completion date | 31/12/2006 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Lower age limit | 18 Years |
| Upper age limit | 60 Years |
| Sex | Not Specified |
| Target number of participants | 100 |
| Key inclusion criteria | 1. Patients undergoing forefoot surgery 2. Aged 18-60years old 3. Able to provide informed consent |
| Key exclusion criteria | 1. Simultaneous iliac crest bone surgery 2. Surgery on the hind foot 3. Patients on long term analgesics for a reason other than foot pain 4. Patients unable to give consent |
| Date of first enrolment | 01/06/2006 |
| Date of final enrolment | 31/12/2006 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
J Block
Oldham
OL1 2JH
United Kingdom
OL1 2JH
United Kingdom
Sponsor information
Record Provided by the NHSTCT Register - 2007 Update - Department of Health
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
Pennine Acute Hospitals NHS Trust
No information available
Own Account
No information available
NHS R&D Support Funding
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
24/10/2016: No publications found, verifying study status with principal investigator
