Betamethasone vs Dextrose Injections in Trigger Finger

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorIstanbul University - Cerrahpasa

About this trial

This study aims to compare the effectiveness of ultrasound-guided betamethasone and dextrose injections in patients with trigger finger.

Trigger finger is a common hand condition characterized by pain, clicking, and locking of the finger due to tendon entrapment at the A1 pulley. Corticosteroid injections are widely used as a first-line treatment; however, they may be associated with potential side effects.

Dextrose injection is an alternative treatment that may promote tissue healing through regenerative mechanisms. However, there is limited high-quality evidence regarding its effectiveness in trigger finger.

In this randomized controlled trial, patients will be assigned to receive either betamethasone or dextrose injection under ultrasound guidance. The primary outcome will be pain intensity measured by the Numeric Rating Scale (NRS). Secondary outcomes will include triggering severity, hand function, grip and pinch strength, and fine motor skills evaluated over a 12-week follow-up period.

The results of this study may help determine whether dextrose injection is a safe and effective alternative to corticosteroid treatment in trigger finger.

Eligibility criteria

Qualifiers

Age between 18 and 75 years

Clinical diagnosis of trigger finger

Presence of symptoms for at least 4 weeks

Disqualifiers

Previous surgery on the affected finger

Injection treatment to the affected finger within the previous 3 months

Active local or systemic infection

Active malignancy

Trial design

Treatments tested in this trial

  • Betamethasone
  • Dextrose Injection

Treatment groups

42 Participants
are divided into 2 treatment groups