Tendinopathy Clinical Trial
Official title:
The Effect of High Volume Injection With and Without Steroid in Chronic Achilles Tendinopathy: A Randomized Double Blinded Prospective Trial
| Verified date | June 2017 |
| Source | Bispebjerg Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aim of the study is to determine the effect of steroid in High Volume Injection (HVI)
compared to HVI without steroid (volume effect) in functional outcomes and ultrasound tendon
thickness and Color Doppler activity in chronic Achilles tendinopathy (AT).
Healthy males with AT will be randomly assigned to either 1) HVI with steroid (50 mls;10 mls
0.5% bupivacaine hydrochloride and 20 mg of Depomedrol followed by 40 ml saline) or 2) HVI
without steroid (50 mls;10 mls 0.5% bupivacaine hydrochloride followed by 40 ml saline).
All subjects will perform a 12-wk eccentric training program with further eccentric training
3 times per week from week 12 to week 24.
Clinical examinations and ultrasound will be performed at baseline (before treatment) with
follow-ups after 6 weeks, 12 weeks and again after 24 weeks prior to baseline to see any
possible changes and differences between the two groups.
| Status | Completed |
| Enrollment | 28 |
| Est. completion date | December 2014 |
| Est. primary completion date | July 2014 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Male |
| Age group | 18 Years to 59 Years |
| Eligibility |
Inclusion Criteria: - Clinically and ultrasound diagnosed unilateral mid-tendinous Achilles tendinopathy. - Symptoms > 3 month Exclusion Criteria: - Bilateral achilles tendinopathy - Insertional tendinopathy - Steroid injections < 12 month - Diabetes or cardiovascular disease - Smoking - Treatment with fluoroquinolones < 6 month |
| Country | Name | City | State |
|---|---|---|---|
| Denmark | Institute of Sportsmedicine, Bispebjerg hospital | Copenhagen |
| Lead Sponsor | Collaborator |
|---|---|
| Bispebjerg Hospital |
Denmark,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The Victorian Institute of Sports Assessment-Achilles questionnaire (VISA-A score) | Changes in VISA-A score over time between the two groups | Baseline, 6 weeks, 12 weeks and 24 weeks | |
| Secondary | The Visual analogue pain scale (VAS score) | Changes in VAS score over time between the two groups | Baseline, 6 weeks, 12 weeks and 24 weeks | |
| Secondary | Ultrasound tendon thickness and color Doppler | Changes in tendon thickness and color Doppler between the two groups | Baseline, 6 weeks, 12 weeks and 24 weeks |
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