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Injection of Hyaluronic Acid Versus Corticosteroid for Treatment of Trigger Finger

D

Dubai Health Authority

Status and phase

Unknown
Early Phase 1

Conditions

Trigger Finger

Treatments

Drug: hyaluronic acid (20 mg/2 mL)
Drug: Triamcinolone acetonide 10mg/ml

Study type

Interventional

Funder types

Other

Identifiers

NCT04645303
DSREC-12/2019_03

Details and patient eligibility

About

The aim of the study is to compare the therapeutic effects of hyaluronic acid versus steroid injections in treating trigger fingers using ultrasound guidance

Full description

A prospective randomized controlled study designed to compare the outcomes of injecting patients with trigger finger with hyaluronic acid versus corticosteroid under ultrasound guidance

Enrollment

100 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult (>18 years)
  • Patients with a clinical diagnosis of trigger finger grade 1-3 on the Quinnell grading scale and confirmed diagnosis by ultrasound.

Exclusion criteria

  • Quinnell's classification grade IV (contracture)
  • Prior injection within 6 months
  • Prior operation of the affected finger
  • Presence of any contracture in the proximal interphalangeal or metacarpophalangeal joint, and
  • History of diabetes, hypothyroidism, and
  • Rheumatic or connective tissue disease
  • Allergy to triamcinolone or hyaluronic acid
  • Pregnancy
  • Secondary triggering e.g. Trauma, infection
  • Trigger finger symptoms duration >6 months

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 2 patient groups

Hyaluronic acid
Experimental group
Description:
1mL of hyaluronic acid (20 mg/2 mL; Hyalgan, Fidia, Abano Terme, Italy) infiltration at A1-Pulley under ultrasound guidance after subcutaneous 2% lidocaine without epinephrine infiltration of the skin overlying the A1-pulley.
Treatment:
Drug: hyaluronic acid (20 mg/2 mL)
Triamcinolone acetonide
Active Comparator group
Description:
1 mL of Triamcinolone acetonide 10mg/ml infiltration at A1-Pulley under ultrasound guidance after subcutaneous 2% lidocaine without epinephrine infiltration of the skin overlying the A1 pulley.
Treatment:
Drug: Triamcinolone acetonide 10mg/ml

Trial contacts and locations

1

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Central trial contact

Mohamed M Abdulla, Consultant; Sahar S Khalil, SSR

Data sourced from clinicaltrials.gov

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