Investigation of treatment of algodystrophy by guanethidine blockade
| ISRCTN | ISRCTN24808507 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN24808507 |
| Secondary identifying numbers | A0053 |
- Submission date
- 07/01/2003
- Registration date
- 07/01/2003
- Last edited
- 14/09/2007
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Musculoskeletal Diseases
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Mr JA Livingstone
Scientific
Scientific
Department of Orthopaedic Surgery
Bristol Royal Infirmary
Marlborough Street
Bristol
BS2 9HW
United Kingdom
| Phone | +44 (0)117 9282658 |
|---|
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 | Not provided at time of registration |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Reflex sympathetic dystrophy |
| Intervention | Intravenous regional (Biers) block to the affected arm using either: 1. 30 ml normal saline, or 2. 15 mg guanethidine in 30 ml 0.5% pritocaine |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | 15 mg guanethidine in 30 ml 0.5% pritocaine |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/01/1999 |
| Completion date | 01/01/2001 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | Not provided at time of registration |
| Key inclusion criteria | Closed, unilateral fracture of the distal radius |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/01/1999 |
| Date of final enrolment | 01/01/2001 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Department of Orthopaedic Surgery
Bristol
BS2 9HW
United Kingdom
BS2 9HW
United Kingdom
Sponsor information
Arthritis Research Campaign (ARC) (UK)
Charity
Charity
Copeman House
St Mary's Court
St Mary's Gate
Chesterfield
Derbyshire
S41 7TD
United Kingdom
| info@arc.org.uk | |
| Website | http://www.arc.org.uk |
"ROR" |
https://ror.org/02jkpm469 |
Funders
Funder type
Charity
Arthritis Research Campaign (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 | 01/04/2002 | Yes | No |
