A double-blind placebo-controlled trial of intra-articular triamcinolone with and without physiotherapy in adhesive capsulitis
| ISRCTN | ISRCTN25152388 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN25152388 |
| Protocol serial number | M0567 |
| Sponsor | Arthritis Research Campaign (ARC) (UK) |
| Funder | Arthritis Research Campaign (UK) |
- Submission date
- 15/07/2002
- Registration date
- 15/07/2002
- Last edited
- 03/10/2007
- 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
Dr Ian Ryans
Scientific
Scientific
Rheumatology Department
Ulster Hospital
Dundonald
BT16 1RH
United Kingdom
| Phone | +44 (0)2890 484511 |
|---|
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | To assess the effectiveness of intra-articular triamcinolone injection and physiotherapy singly or combined in the treatment of adhesive capsulitis of the shoulder. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Adhesive capsulitis of the shoulder |
| Intervention | 1. Intra-articular triamcinolone and physiotherapy 2. Intra-articular triamcinolone without physiotherapy 3. Intra-articular placebo and physiotherapy 4. Intra-articular placebo without physiotherapy |
| Intervention type | Drug |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | Triamcinolone |
| Primary outcome measure(s) | Not provided at time of registration |
| Key secondary outcome measure(s) | Not provided at time of registration |
| Completion date | 01/04/2002 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Key inclusion criteria | Painful shoulder for more than 4 weeks and less than 6 months with greater than 25% limitation of active and passive range of movement in external rotation and abduction as compared with the contralateral shoulder. |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/10/1998 |
| Date of final enrolment | 01/04/2002 |
Locations
Countries of recruitment
- United Kingdom
- Northern Ireland
Study participating centre
Rheumatology Department
Dundonald
BT16 1RH
United Kingdom
BT16 1RH
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | 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 | 01/04/2005 | Yes | No |
