Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT04895956

Intra-sheath vs Extra-sheath Injection for De Quervain's Tenosynovitis

Led by University of California, Davis · Updated on 2026-02-12

80

Participants Needed

1

Research Sites

227 weeks

Total Duration

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AI-Summary

What this Trial Is About

The aim of the study is to determine whether or not extra-sheath steroid injections are inferior to intra-sheath steroid injections in the treatment of DeQuervain's Tenosynovitis. Patients will be randomized to either the intra-sheath group or the extra-sheath group and their pre-injection level of pain will be assessed using the visual analog scale. Appropriate injections will then be administered by 1 of 3 UC Davis hand surgeons. Six weeks post injection the patients will be reassessed using the visual analog scale and their score at 6 weeks will be compared to their pre-injection score.

CONDITIONS

Official Title

Intra-sheath vs Extra-sheath Injection for De Quervain's Tenosynovitis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent from the patient exclusively and not a legal representative
  • Clinically diagnosed with De Quervain's
  • VAS score of at least 40mm pre-injection
  • Life expectancy greater than 1 year
Not Eligible

You will not qualify if you...

  • Previously received steroid injection for De Quervain's
  • Previously had surgery for De Quervain's in the affected wrist
  • Previously had steroid injection and failed treatment for trigger finger
  • Allergic to lidocaine or dexamethasone
  • Have serious medical conditions that increase risk
  • Past history of hypothyroidism or rheumatoid arthritis
  • Pregnant women
  • Prisoners

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UC Davis Health, Department of Orthopaedics

Sacramento, California, United States, 95817

Actively Recruiting

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Research Team

J

Julia Martin, MS

CONTACT

C

Christopher O Bayne, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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