Trigger finger. Trigger finger, unspecified finger
Conditions
Interventions
Target group consists of 19 Trigger finger patients. Every patient will be treated by Extra Corporal Shock Wave Therapy for 3 weeks (1 week interval between sessions). Radial head protocol includes 10
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Trigger finger, grade 1 or more
Exclusion criteria
Exclusion criteria: Previous treatment in less than last 6 months, including corticosteroid injection or surgical release Bleeding disorders Pregnancy Malignancy Local infection Arrhythmia and cardiac pace maker
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity due to Visual Analogue Scale (0-10). Timepoint: Pain intensity due to Visual Analogue Scale system, before, immediately after, 6 weeks and 18 weeks after treatment. Method of measurement: Visual Analogue Scale (0-10).;Trigger finger grading: due to Quinnell Trigger finger score. Timepoint: Before, immediately after, 6 weeks and 18 weeks after treatment. Method of measurement: Quinnell Trigger finger score.;Dysfunction: due to Quick Disability of Arm, Shoulder and Hand System. Timepoint: Before, immediately after, 6 weeks and 18 weeks after treatment. Method of measurement: Quick Disability of Arm, Shoulder and Hand System. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFahime Momeni
Esfahan University of Medical Sciences
Outcome results
None listed