RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2022-01-24
Study Completion:2025-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04895956

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Signed informed consent from the patient exclusively and not a legal representative
  2. * Clinically diagnosed with De Quervain's
  3. * VAS score of at least 40mm pre-injection
  4. * Life expectancy greater than 1 year
  1. * Having previously undergone steroid injection in the treatment of De Quervain's
  2. * Having previously undergone surgery for De Quervain's in the affected wrist
  3. * Having previously undergone steroid injection and failed in the treatment of trigger finger
  4. * Allergies to lidocaine or dexamethasone
  5. * Underlying serious medical conditions that would place the patient at risk
  6. * Past history of hypothyroidism or rheumatoid arthritis
  7. * Pregnant women
  8. * Prisoners

Contacts and Locations

Study Contact

Julia Martin, MS
CONTACT
916-7348175
jyhmartin@ucdavis.edu
Christopher O Bayne, MD
CONTACT
(916) 734-2700
cbayne@ucdavis.edu

Principal Investigator

Christopher O Bayne, MD
PRINCIPAL_INVESTIGATOR
University of California, Davis

Study Locations (Sites)

UC Davis Health, Department of Orthopaedics
Sacramento, California, 95817
United States

Collaborators and Investigators

Sponsor: University of California, Davis

  • Christopher O Bayne, MD, PRINCIPAL_INVESTIGATOR, University of California, Davis

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-01-24
Study Completion Date2025-06-01

Study Record Updates

Study Start Date2022-01-24
Study Completion Date2025-06-01

Terms related to this study

Keywords Provided by Researchers

  • Steroid injection

Additional Relevant MeSH Terms

  • De Quervain Tenosynovitis