Smith 2001.
Methods |
Study design: RCT Duration of the study: not reported Protocol was published before recruitment of participants: not reported Details of trial registration: not reported Funding sources: not reported |
Participants |
Place of study: Tennesse, USA Number of participants assigned: 100 participants Number of participants assessed: 65 participants (30 surgical; 35 conservative) Inclusion criteria
Exclusion criteria: not reported Age: not reported Classification of injury: not reported |
Interventions |
Timing of intervention: not reported: participants with acute fractures Type of surgical intervention: open reduction and plate fixation with limited contact dynamic compression plates Type of conservative intervention: simple sling or figure‐of‐eight bandage Rehabilitation: not reported Any co‐interventions: not reported |
Outcomes |
Length of follow‐up: until radiographic union or non‐union, surgical group (mean/range): 16/8‐28 months; conservative group (mean/range): 18.6/8‐32 months Loss to follow‐up: 35 participants were lost to follow‐up Primary outcomes
Secondary outcomes Treatment failure measured by:
Adverse events measured by:
|
Notes | We tried unsuccessfully to contact the study authors to obtain further information. This trial was presented in 2001 at a conference, and it is unlikely that the full results will ever be published. |
DASH: Disability of the Arm, Shoulder, and Hand questionnaire; LCP: locking compression plate; RCT: randomised controlled trial