Eutrophic stimulation following primary nerve repair - an evaluation
| ISRCTN | ISRCTN75177927 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN75177927 |
| Secondary identifying numbers | RHC18049 |
- Submission date
- 23/01/2004
- Registration date
- 23/01/2004
- Last edited
- 13/01/2010
- Recruitment status
- Stopped
- Overall study status
- Stopped
- Condition category
- Injury, Occupational Diseases, Poisoning
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
Mrs Catherine Bucher
Scientific
Scientific
University of Keele
Dept of Physiotherapy Studies
Keele University
Keele
ST5 5BG
United Kingdom
| Phone | +44 (0)1782 584192 |
|---|---|
| pta06@keele.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 | |
| Study objectives | This study aims to gain preliminary evidence to support or refute the inclusion of eutrophic stimulation in a rehabilitation programme following primary repair of Median and/or Ulnar nerves at wrist level. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Primary nerve repair |
| Intervention | 1. Eutrophic stimulation 2. Standard treatment |
| Intervention type | Other |
| Primary outcome measure | The primary outcome measure will be the two point discrimination test (sensibility). Subjects will be assessed in terms of sensibility, range of motion, motor and functional recovery using valid and reliable clinical assessment methods. Results may generate related research in both the field of hand trauma and peripheral nerve injury. Future studies may determine such things as optimum stimulation parameters. |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/09/1997 |
| Completion date | 01/09/1999 |
| Reason abandoned (if study stopped) | Participant recruitment issue |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Both |
| Target number of participants | Not provided at time of registration |
| Key inclusion criteria | Subjects will be drawn from the Burns and Plastic Surgery Unit, Withington Hospital over an eighteen month to two year period. |
| Key exclusion criteria | Does not match inclusion criteria |
| Date of first enrolment | 01/09/1997 |
| Date of final enrolment | 01/09/1999 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
University of Keele
Keele
ST5 5BG
United Kingdom
ST5 5BG
United Kingdom
Sponsor information
NHS R&D Regional Programme Register - 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.doh.gov.uk |
Funders
Funder type
Government
NHS Executive North West (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 |
