Trigger finger Trigger finger, 448 kHz Radiofrequency
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients aged between 18 and 60 years. 2. Diagnosis of trigger finger with severity levels 1or2or 3 based on Green classification. 3.No use of pain-relieving medications within two weeks prior to study enrollment. 4.No steroid injections in the tendon sheath within three months prior to study enrollment. 5.Willing and able to participate in the study.
Exclusion criteria
Exclusion criteria: 1.Participants who are contraindicated for radiofrequency treatment, including pregnant or breastfeeding women, and those with implanted metal or electronic devices such as pacemakers. 2.Presence of open wounds at the intended treatment site. 3.Diagnosis of cancer. 4.Thrombophlebitis. 5. Patients with sensory impairments (congenital, nerve damage, hemiplegia, or quadriplegia) or those taking medications that alter sensory perception.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score Week3 ,week5 ,week7 and week9 after treatment Visual analogue scale | — |
Secondary
| Measure | Time frame |
|---|---|
| Physical function Week3 ,week5 ,week7 and week9 after treatment QuickDASH Thai version | — |
Countries
Thailand
Contacts
Department of Anti-aging and Regenerative Science Collage of Integrative Medicine