Low-Level Laser Therapy for Trigger Finger
Official title: Effectiveness of Low-Level Laser Therapy for Trigger Finger: A Randomized Double-Blind Sham-Controlled Trial
Run by Dokuz Eylul University · NCT07753460 · Data updated 2026-11-12
This study tests whether low-level laser therapy can help people with trigger finger see if it reduces pain and improves finger movement.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 91 (estimated) |
| Sponsor | Dokuz Eylul University Academic / other |
| Locations | 1 site (Izmir, Balçova) |
| Status | Recruiting |
| Started | August 7, 2025 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | September 30, 2026 |
| Trial ID | NCT07753460 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with a clinical diagnosis of trigger finger who are treated as outpatients at Dokuz Eylül University and meet eligibility criteria.
✕Probably not a fit
Patients with fixed deformities, recent splint/therapy/steroid treatment, prior surgery on the affected finger, or other excluded conditions may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study compares low-level laser therapy (LLLT) with sham LLLT in people with trigger finger (stenosing tenosynovitis). Participants receive either active LLLT or a placebo procedure to determine if LLLT provides benefit beyond sham therapy. Outcomes focus on pain, triggering, and finger function, with a clinically diagnosed trigger finger setting. The trial is conducted at Dokuz Eylül University in Izmir, Turkey, with specific inclusion and exclusion criteria to select appropriate adult participants. Safety monitoring and adherence to standard clinical practices are included to ensure proper conduct of the intervention.
Why it matters
Potential benefit: If successful, patients may experience reduced finger triggering and pain, leading to improved hand function.
How similar studies have gone: Existing evidence for LLLT in trigger finger is limited, with small or nonrandomized prior reports; this study adds controlled data.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Applying to the outpatient clinic of the Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Dokuz Eylül University * A clinical diagnosis of trigger finger based on typical pain and tenderness over the A1 pulley accompanied by triggering of the affected finger * Willingness to participate in the study Exclusion Criteria: * Multiple trigger fingers in the same hand * Fixed deformity (Quinnell grade 4) * Splint treatment, physical therapy, or steroid injection for the affected trigger finger within the previous 6 months * Previous surgery for the affected trigger finger * Musculoskeletal disorders or peripheral nerve injury involving the ipsilateral upper extremity * Rheumatoid arthritis, carpal tunnel syndrome, Dupuytren disease, amyloidosis, or mucopolysaccharidosis * Active infection, bleeding, skin lesions, or an implant at the treatment site * Radiotherapy within the previous 6 months * Photodermatosis, photosensitivity, or systemic lupus erythematosus * Pregnancy, epilepsy, coagulopathy, active malignancy, or the presence of a cardiac pacemaker * Cognitive impairment that precludes understanding of the study questionnaires.
Where it's running
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Dokuz Eylul University
Izmir, Balçova, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Gözde Kırım Kaya, MD
- Email: gozde.kirimkaya@deu.edu.tr
- Phone: +902324123951
Similar studies
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Longitudinal versus transverse A1 pulley incision for trigger finger
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.