Infra clavicular plexus block - Lateral (coracoid) approach vs vertical approach - a comparison of techniques
| ISRCTN | ISRCTN73554324 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN73554324 |
| Secondary identifying numbers | N0249142464 |
- Submission date
- 30/09/2005
- Registration date
- 30/09/2005
- Last edited
- 18/10/2017
- 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
Dr Matthew Oldman
Scientific
Scientific
Specialist Registrar in Anaesthesia
Dept of Anaesthesia
Taunton & Somerset Hospital
Taunton
TA1 5DA
United Kingdom
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Not specified |
| Study type | Not Specified |
| Participant information sheet | Not available in web format, please use the contact details below to request a patient information sheet |
| Scientific title | Infra clavicular plexus block - Lateral (coracoid) approach vs vertical approach - a comparison of techniques |
| Study objectives | Which of two infraclavicular approaches to the brachial plexus is preferable |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Surgery: Arm |
| Intervention | Randomised Controlled Trial: 1. Lateral approach 2. Vertical approach |
| Intervention type | Procedure/Surgery |
| Primary outcome measure | Degree of sensory block, complications |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/12/2001 |
| Completion date | 09/09/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Not Specified |
| Target number of participants | 40 |
| Key inclusion criteria | 40 patients undergoing distal upper limb surgery |
| Key exclusion criteria | 1. Age under 16 2. Uunable to give informed consent 3. Neurovascular compromise of limb 4. Allergy to amide local anaesthetic agents 5. Coagulopathy (INR>2) 6. Chest or shoulder deformities 7. Healed but disclosed clavicle fracture |
| Date of first enrolment | 01/12/2001 |
| Date of final enrolment | 09/09/2004 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Specialist Registrar in Anaesthesia
Taunton
TA1 5DA
United Kingdom
TA1 5DA
United Kingdom
Sponsor information
Department of Health
Government
Government
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
Hospital/treatment centre
Taunton and Somerset Research and Development Consortium (UK)
No information available
NHS R&D Support Funding (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
18/10/2017: No publications found, study status unverified.
