The BOND study is a prospective, randomised single blinded controlled trial to assess the effect of night splinting in patients who have had collagenase injection and manipulation therapy for Dupuytren's Contracture.
This trial will assess the effectiveness of night splinting in Dupuytrens' contracture on functional and quality of life outcomes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Thermoplastic Night splint created and moulded to the individual patients hand in-house using generic thermoplastic.
Royal Liverpool & Broadgreen University Hospitals NHS Trust
Liverpool, Merseyside, United Kingdom
Range of motion
To assess change in range of motion measured in degrees between pre-treatment, immediately post-treatment, 12 weeks post-treatment and 12 months post-treatment
Time frame: At 0 weeks, 12 weeks and 52 weeks
PEM Questionnaire
Patient Evaluation Measure to give disability score
Time frame: At 0 weeks, 12 weeks and 52 weeks
URAM Questionnaire
Hand specific outcome questionnaire to assess quality of life outcomes
Time frame: At 0 weeks, 12 weeks and 52 weeks
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