A true to life study of pain management early in rotator cuff tendonitis and adhesive capsulitis
| ISRCTN | ISRCTN20861284 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN20861284 |
| Secondary identifying numbers | N0080151784 |
- Submission date
- 30/09/2005
- Registration date
- 30/09/2005
- Last edited
- 08/04/2014
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Signs and Symptoms
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 Alan Hakim
Scientific
Scientific
Consultant Rheumatologist
Whipps Cross University Hospital Trust
Whipps Cross Hospital
Whipps Cross Road
London
E11 1NR
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 |
| Scientific title | |
| Study objectives | To determine whether early intervention with corticosteroid injection is effective in reducing acute pain from rotator cuff tendonitis or adhesive capsulitis. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Signs and Symptoms: Pain |
| Intervention | Randomised study |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | Corticosteroids |
| Primary outcome measure | To measure the change in perceived pain and disability to inform treatment decisions and improve the evidence base for care of patients with this condition. |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/11/2004 |
| Completion date | 01/08/2006 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target number of participants | 150 |
| Key inclusion criteria | 150 patients |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/11/2004 |
| Date of final enrolment | 01/08/2006 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Consultant Rheumatologist
London
E11 1NR
United Kingdom
E11 1NR
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
Government
Whipps Cross University Hospital NHS Trust (UK)
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 |
