"Is a simultaneaus intervention of triamcinolon injections with standardized isometric exercises more effective compared to the usual care according to the NHG standard in patients with shoulder complaints. A prospective, singel blind, randomized clinical trial."

"Is a simultaneaus intervention of triamcinolon injections with standardized isometric exercises more effective compared to the usual care according to the NHG standard in patients with shoulder complaints. A prospective, singel blind, randomized clinical trial." - Investigation of the efficacy of shoulder injections

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON29758

Enrollment

205

Registered

2006-12-13

Start date

2007-09-15

Completion date

Unknown

Last updated

2024-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

"impingement subacromial" "tendinitis"

Interventions

group A a simultaneus intervention in which the patients will be injected with a combination of lidocaine and 1 ml Kenacort A40 and at the same time exercises

and group B in which the patient will be injected with a combination of lidocaine and 1 ml Kenacort A40 and after six weeks according to the NHG-standard with exercises.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Those patients with shoulder complaints consulting ther GP with complaints also during the night, and presence of painfull-arc and restricted range of motion.

Exclusion criteria

Exclusion criteria: not signed informed consent form, age under 18 or above 70 year, treatment (exercises or corticosteroid injections) of shoulder complaints during the last 6 months, insufficient command of the Dutch language, spoken and/or written.

Design outcomes

Primary

Measure	Time frame
The primary outcome is the change in pain in rest, during activities or during the night of the last 24 hours, between baseline and 78 weeks.	—

Secondary

Measure	Time frame
Change compared to the baselien assessments of: - DASH questionnaire, - SF36 questionnaire, - Analgetica use, - Participant rated improvement, - Range of Motion maesurements, - Painful-Arc, - complications of injections.	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)