University of Connecticut Health Center
Farmington, Connecticut, 06030, United States
NCT Number: NCT01310218
The purpose of the study is to prospectively compare the functional, satisfaction, and wound outcomes of patients treated with one of two accepted methods of postoperative dressing following carpal tunnel release. Hypothesis: There will be no difference between the short term (approximately 2 - 3 days)and longer term (9 to 14 days)bulky dressing groups in terms of outcomes.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 4
Farmington, Connecticut, 06030, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
2 weeks of bulky dressing
2 days bulky dressing followed by bandaid
Time frame: Levine-Katz Scale at baseline (pre-operation)
Symptom and function of Carpal Tunnel Syndrome
Time frame: Baseline and two weeks.
Symptom and Function of Carpal Tunnel Syndrome
Time frame: Baseline and three months.
Symptom and function of Carpal Tunnel Syndrome
Looking for future studies?
Notify MeUConn Health
Other
Length of Postoperative Dressing After Mini-open Carpal Tunnel Release: A Randomized Prospective Comparison
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