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. 2003 Jan 20;2003(1):CD004016. doi: 10.1002/14651858.CD004016

Strobel 1996.

Methods Randomised controlled trial reported in German. 
 Blinding: unclear 
 Loss to follow‐up: 3(15%) in placebo group and and 6(30%) in steroid injection group did not participate in follow up 
 Appropriate statistical analysis: not intention to treat analysis, completers analysis only
Participants 40 patients 
 Inclusion criteria: 
 chronic painful shoulder caused by chronic subacromial bursitis or supraspinatus tendinitis ‐ criteria for diagnoses not reported 
 Exclusion criteria: 
 not stated
Interventions Group 1(20 patients): 5ml 0.5% mepivacainhydrochloride (MVH) 
 injection 
 Group 2(20 patients): 5ml 0.5% MVH plus 20mg triamcinolone hexacetonid (THA) injection
Outcomes Assessed at baseline, 14, 90 and 360 days 
 1) Pain (either no pain, low pain, strong pain, very strong pain) 
 2) angle of abduction reported by patient after eduction in front of a mirror 
 3) work status
Notes Met inclusion criteria for review but insufficient data presented (ie. no measure of variance or data from which it could be calculated), therefore not included in meta‐analysis. 
 Reported greater reduction in pain in placebo group at 90 and 360 days but more patients in treated group were able to work after one year.
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear